A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596797



Internal ID6984111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:83631093..83637800hg38UCSC Ensembl
Innerchr3:83631094..83637799hg38UCSC Ensembl
Outerchr3:83631092..83637801hg38UCSC Ensembl
chr3:83680244..83686951hg19UCSC Ensembl
Innerchr3:83680245..83686950hg19UCSC Ensembl
Outerchr3:83680243..83686952hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg386708
hg196708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11058817, essv11058815, essv11058816
SamplesHG02052, HG01756, NA11832
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596797
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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