A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10980997



Internal ID6654223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36549578..36551822hg38UCSC Ensembl
Innerchr3:36549628..36551772hg38UCSC Ensembl
Outerchr3:36549480..36551920hg38UCSC Ensembl
chr3:36591070..36593314hg19UCSC Ensembl
Innerchr3:36591120..36593264hg19UCSC Ensembl
Outerchr3:36590972..36593412hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382245
hg192245
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595867
Supporting Variants
SamplesNA20803
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10980997
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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