A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9896297



Internal ID3992847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31980082..31981782hg38UCSC Ensembl
Innerchr1:31980115..31981750hg38UCSC Ensembl
Outerchr1:31980050..31981815hg38UCSC Ensembl
chr1:32445683..32447383hg19UCSC Ensembl
Innerchr1:32445716..32447351hg19UCSC Ensembl
Outerchr1:32445651..32447416hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585658
Supporting Variants
SamplesHG03644
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9896297
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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