A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633150



Internal ID7019960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91249676..91252589hg38UCSC Ensembl
Innerchr13:91249678..91252587hg38UCSC Ensembl
Outerchr13:91249674..91252591hg38UCSC Ensembl
chr13:91901930..91904843hg19UCSC Ensembl
Innerchr13:91901932..91904841hg19UCSC Ensembl
Outerchr13:91901928..91904845hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg382914
hg192914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14848484, essv14848463, essv14848461, essv14848504, essv14848489, essv14848488, essv14848478, essv14848481, essv14848476, essv14848480, essv14848465, essv14848466, essv14848471, essv14848472, essv14848483, essv14848501, essv14848495, essv14848469, essv14848467, essv14848475, essv14848492, essv14848485, essv14848486, essv14848455, essv14848502, essv14848477, essv14848458, essv14848460, essv14848464, essv14848470, essv14848473, essv14848487, essv14848482, essv14848491, essv14848503, essv14848496, essv14848493, essv14848498, essv14848456, essv14848457, essv14848479, essv14848500, essv14848505, essv14848494, essv14848490, essv14848462, essv14848497, essv14848474, essv14848499, essv14848468, essv14848459
SamplesHG02574, HG02890, HG03175, HG03111, HG03115, NA19350, NA19092, NA18486, HG03126, HG02769, NA19171, HG03168, HG03099, NA18923, HG02595, HG03105, HG02111, HG03826, HG02634, NA19238, HG02885, NA19159, HG02427, HG02477, HG01183, NA19908, HG03363, HG03027, HG01392, HG03085, NA19461, NA19118, HG02817, HG03451, HG03046, HG03354, HG02332, HG02586, NA19324, NA19310, HG02839, HG02580, HG01086, HG03565, NA20348, HG03112, HG02462, HG02768, HG02465, NA19153, HG03271
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633150
Frequency
Sample Size2504
Observed Gain0
Observed Loss51
Observed Complex0
Frequencyn/a


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