A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13538760



Internal ID6111742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82257311..82264381hg38UCSC Ensembl
Innerchr9:82257311..82264381hg38UCSC Ensembl
Outerchr9:82257004..82264689hg38UCSC Ensembl
chr9:84872226..84879296hg19UCSC Ensembl
Innerchr9:84872226..84879296hg19UCSC Ensembl
Outerchr9:84871919..84879604hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg387071
hg197071
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620884
Supporting Variants
SamplesNA19651
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13538760
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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