A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635645



Internal ID7022443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105473682..105484540hg38UCSC Ensembl
chr14:105940019..105950877hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3810859
hg1910859
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15117483, essv15117441, essv15117523, essv15117412, essv15117462, essv15117531, essv15117507, essv15117445, essv15117461, essv15117500, essv15117482, essv15117526, essv15117489, essv15117426, essv15117468, essv15117506, essv15117438, essv15117493, essv15117417, essv15117423, essv15117419, essv15117415, essv15117420, essv15117457, essv15117521, essv15117495, essv15117431, essv15117450, essv15117509, essv15117446, essv15117443, essv15117497, essv15117510, essv15117427, essv15117451, essv15117480, essv15117456, essv15117520, essv15117448, essv15117524, essv15117491, essv15117429, essv15117496, essv15117481, essv15117428, essv15117430, essv15117511, essv15117422, essv15117458, essv15117470, essv15117436, essv15117533, essv15117475, essv15117418, essv15117535, essv15117530, essv15117424, essv15117494, essv15117518, essv15117484, essv15117536, essv15117525, essv15117512, essv15117465, essv15117432, essv15117534, essv15117519, essv15117447, essv15117449, essv15117504, essv15117434, essv15117413, essv15117476, essv15117437, essv15117522, essv15117466, essv15117439, essv15117513, essv15117469, essv15117464, essv15117501, essv15117452, essv15117499, essv15117527, essv15117517, essv15117471, essv15117433, essv15117492, essv15117478, essv15117508, essv15117444, essv15117503, essv15117416, essv15117488, essv15117485, essv15117472, essv15117442, essv15117486, essv15117474, essv15117487, essv15117435, essv15117490, essv15117528, essv15117440, essv15117516, essv15117505, essv15117529, essv15117459, essv15117537, essv15117515, essv15117514, essv15117498, essv15117411, essv15117477, essv15117479, essv15117455, essv15117421, essv15117532, essv15117460, essv15117425, essv15117454, essv15117453, essv15117463, essv15117414, essv15117502, essv15117473, essv15117467
SamplesNA18997, NA18998, NA18745, NA20339, NA19028, NA21111, NA19794, HG02002, NA18647, HG01348, HG00351, NA19734, NA18979, NA18999, NA18641, NA19795, NA18639, NA20298, HG02277, HG00452, NA19314, HG00097, HG02285, NA19067, HG00356, NA12812, HG01702, HG02140, HG02485, HG02087, HG01277, NA19307, HG00129, NA18574, HG00851, NA18642, NA21108, HG00451, NA19038, HG02278, HG02131, HG00130, NA19923, NA19041, HG00335, HG02003, NA21109, HG01628, NA18560, NA18748, HG02082, NA21107, HG02138, HG00406, HG02104, NA18985, HG01626, NA18640, HG00419, NA21105, NA19027, HG02134, NA21106, NA18645, NA18538, NA18525, HG01104, HG02090, HG00428, NA12872, NA19086, HG01344, NA19984, NA19184, HG02084, NA18939, HG01345, NA18910, HG02508, HG02497, NA21116, NA18757, HG01619, HG00479, HG00350, NA21112, NA19031, HG02141, NA19001, NA19752, NA19740, HG02081, HG02286, HG00099, HG01625, HG00376, HG02484, HG01700, HG00128, NA19035, HG00407, NA19308, HG00382, HG02089, NA19309, HG00383, NA18535, NA19149, NA19735, HG02088, NA12873, NA20351, HG01623, NA19310, HG01620, NA18643, NA12874, HG01086, HG00421, HG00378, HG01085, HG02239, HG00234, NA19096, HG00345, NA18740, HG01618
Known GenesCRIP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635645
Frequency
Sample Size2504
Observed Gain127
Observed Loss0
Observed Complex0
Frequencyn/a


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