A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13571856



Internal ID3573673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95274100..95276023hg38UCSC Ensembl
Innerchr9:95274107..95276017hg38UCSC Ensembl
Outerchr9:95274094..95276030hg38UCSC Ensembl
chr9:98036382..98038305hg19UCSC Ensembl
Innerchr9:98036389..98038299hg19UCSC Ensembl
Outerchr9:98036376..98038312hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381924
hg191924
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621150
Supporting Variants
SamplesNA20505
Known GenesFANCC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13571856
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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