A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615361



Internal ID7002250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146096107..146098048hg38UCSC Ensembl
Innerchr7:146096163..146097992hg38UCSC Ensembl
Outerchr7:146096051..146098104hg38UCSC Ensembl
chr7:145793200..145795141hg19UCSC Ensembl
Innerchr7:145793256..145795085hg19UCSC Ensembl
Outerchr7:145793144..145795197hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg381942
hg191942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12997597, essv12997606, essv12997581, essv12997576, essv12997607, essv12997594, essv12997587, essv12997586, essv12997599, essv12997601, essv12997580, essv12997584, essv12997602, essv12997578, essv12997583, essv12997603, essv12997579, essv12997608, essv12997588, essv12997592, essv12997589, essv12997600, essv12997604, essv12997585, essv12997605, essv12997591, essv12997582, essv12997593, essv12997595, essv12997590, essv12997598, essv12997577, essv12997596
SamplesHG03121, HG02852, HG02836, NA19020, NA20294, NA19819, NA19393, HG00737, HG03082, HG01503, NA19448, HG02840, HG02860, HG03479, NA20291, NA19038, NA19024, NA19901, HG03073, HG01882, NA19461, HG02817, HG03388, HG02594, HG03539, HG02611, NA19360, HG03066, NA19351, HG02646, NA19213, NA18522, HG02629
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615361
Frequency
Sample Size2504
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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