A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644218



Internal ID7030974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34818073..34818802hg38UCSC Ensembl
Innerchr19:34818075..34818800hg38UCSC Ensembl
Outerchr19:34818071..34818804hg38UCSC Ensembl
chr19:35308977..35309706hg19UCSC Ensembl
Innerchr19:35308979..35309704hg19UCSC Ensembl
Outerchr19:35308975..35309708hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16044841, essv16044830, essv16044820, essv16044812, essv16044811, essv16044823, essv16044814, essv16044815, essv16044824, essv16044843, essv16044839, essv16044842, essv16044837, essv16044829, essv16044827, essv16044835, essv16044816, essv16044810, essv16044825, essv16044822, essv16044831, essv16044844, essv16044817, essv16044832, essv16044818, essv16044828, essv16044840, essv16044838, essv16044834, essv16044836, essv16044833, essv16044813, essv16044826, essv16044821, essv16044819
SamplesHG01985, HG02574, NA19222, NA19794, NA19204, NA19914, HG01971, HG01177, HG02595, HG02645, HG03268, NA20340, NA19207, NA19385, HG02588, NA19200, HG03270, HG01171, HG03061, HG01122, HG02511, HG02757, HG02817, HG01241, NA20282, NA19756, NA19395, NA18858, HG01896, NA18517, HG02308, HG01551, NA20281, HG03376, HG02465
Known GenesLOC400685
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644218
Frequency
Sample Size2504
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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