A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692234



Internal ID15082200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124262893..124357163hg38UCSC Ensembl
Innerchr9:127025172..127119442hg19UCSC Ensembl
Innerchr9:126064993..126159263hg18UCSC Ensembl
Innerchr9:124104726..124198996hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3894271
hg1994271
hg1894271
hg1794271
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519767
Supporting Variants
Samples
Known GenesLOC100129034, NEK6, PSMB7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692234
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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