A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654110



Internal ID15390762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149761534..149813061hg38UCSC Ensembl
Innerchr7:149458623..149510149hg19UCSC Ensembl
Innerchr7:149089556..149141082hg18UCSC Ensembl
Innerchr7:148896271..148947797hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3851528
hg1951527
hg1851527
hg1751527
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517242
Supporting Variants
Samples
Known GenesSSPO, ZNF467
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654110
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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