A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621141



Internal ID6661321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94901407..94904588hg38UCSC Ensembl
Innerchr9:94901408..94904587hg38UCSC Ensembl
Outerchr9:94901406..94904589hg38UCSC Ensembl
chr9:97663689..97666870hg19UCSC Ensembl
Innerchr9:97663690..97666869hg19UCSC Ensembl
Outerchr9:97663688..97666871hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg383182
hg193182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13571505, essv13571507, essv13571506
SamplesHG03064, HG03485, HG03464
Known GenesC9orf3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621141
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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