A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10987885



Internal ID6678692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39769528..39780124hg38UCSC Ensembl
Innerchr3:39769528..39780124hg38UCSC Ensembl
Outerchr3:39769028..39780624hg38UCSC Ensembl
chr3:39811019..39821615hg19UCSC Ensembl
Innerchr3:39811019..39821615hg19UCSC Ensembl
Outerchr3:39810519..39822115hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3810597
hg1910597
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595937
Supporting Variants
SamplesNA20812
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10987885
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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