A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597936



Internal ID6985073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139284898..139286500hg38UCSC Ensembl
Innerchr3:139284900..139286499hg38UCSC Ensembl
Outerchr3:139284897..139286502hg38UCSC Ensembl
chr3:139003740..139005342hg19UCSC Ensembl
Innerchr3:139003742..139005341hg19UCSC Ensembl
Outerchr3:139003739..139005344hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381603
hg191603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11160821, essv11160815, essv11160825, essv11160819, essv11160823, essv11160820, essv11160824, essv11160817, essv11160822, essv11160816, essv11160826, essv11160818
SamplesNA19394, NA18508, HG02798, NA18519, HG03045, HG02477, HG01390, NA18912, NA19257, HG03259, HG02763, NA19463
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597936
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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