A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703631



Internal ID15440283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129316498..129323014hg38UCSC Ensembl
Innerchr9:132078777..132085293hg19UCSC Ensembl
Innerchr9:131118598..131125114hg18UCSC Ensembl
Innerchr9:129158331..129164847hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386517
hg196517
hg186517
hg176517
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527231
Supporting Variants
Samples
Known GenesC9orf106
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703631
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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