A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705038



Internal ID15441690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16570144..16581969hg38UCSC Ensembl
Innerchr9:16570142..16581967hg19UCSC Ensembl
Innerchr9:16560142..16571967hg18UCSC Ensembl
Innerchr9:16560142..16571967hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3811826
hg1911826
hg1811826
hg1711826
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528443
Supporting Variants
Samples
Known GenesBNC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705038
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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