A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13630794



Internal ID1053074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131320626..131326932hg38UCSC Ensembl
Innerchr9:131321126..131326432hg38UCSC Ensembl
Outerchr9:131319626..131327932hg38UCSC Ensembl
chr9:134196013..134202319hg19UCSC Ensembl
Innerchr9:134196513..134201819hg19UCSC Ensembl
Outerchr9:134195013..134203319hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg386307
hg196307
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621878
Supporting Variants
SamplesHG00674
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13630794
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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