A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696755



Internal ID15433407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107180884..107192531hg38UCSC Ensembl
Innerchr9:109943165..109954812hg19UCSC Ensembl
Innerchr9:108982986..108994633hg18UCSC Ensembl
Innerchr9:107022720..107034367hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3811648
hg1911648
hg1811648
hg1711648
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519264
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696755
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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