A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638750



Internal ID7025535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59622654..59625816hg38UCSC Ensembl
Innerchr16:59622804..59625666hg38UCSC Ensembl
Outerchr16:59622504..59625966hg38UCSC Ensembl
chr16:59656558..59659720hg19UCSC Ensembl
Innerchr16:59656708..59659570hg19UCSC Ensembl
Outerchr16:59656408..59659870hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383163
hg193163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15492727, essv15492702, essv15492721, essv15492715, essv15492709, essv15492730, essv15492729, essv15492724, essv15492704, essv15492723, essv15492708, essv15492713, essv15492711, essv15492726, essv15492700, essv15492720, essv15492717, essv15492710, essv15492705, essv15492719, essv15492712, essv15492722, essv15492707, essv15492703, essv15492725, essv15492706, essv15492699, essv15492716, essv15492714, essv15492728, essv15492701, essv15492718
SamplesHG02628, HG03548, NA19119, NA19916, HG03246, HG03105, HG02111, HG03079, HG02461, NA19159, NA19239, HG02477, HG03301, HG01474, NA19452, NA18858, HG02255, HG02667, HG02799, NA19037, HG02837, NA19439, HG02771, HG03565, HG02974, HG03538, HG01914, NA19430, NA19463, NA18522, HG03265, HG02760
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638750
Frequency
Sample Size2504
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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