A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671339



Internal ID15061305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76432201..76450383hg38UCSC Ensembl
Innerchr9:79047117..79065299hg19UCSC Ensembl
Innerchr9:78236937..78255119hg18UCSC Ensembl
Innerchr9:76276671..76294853hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3818183
hg1918183
hg1818183
hg1718183
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520423
Supporting Variants
Samples
Known GenesGCNT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671339
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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