A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13464670



Internal ID3466486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38498775..38685339hg38UCSC Ensembl
Innerchr9:38498816..38685298hg38UCSC Ensembl
Outerchr9:38498734..38685380hg38UCSC Ensembl
chr9:38498772..38685336hg19UCSC Ensembl
Innerchr9:38498813..38685295hg19UCSC Ensembl
Outerchr9:38498731..38685377hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38186565
hg19186565
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620429
Supporting Variants
SamplesNA12872
Known GenesANKRD18A, FAM201A, FAM95C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13464670
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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