A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698446



Internal ID15435098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1121522..1152053hg38UCSC Ensembl
Innerchr7:1161158..1191689hg19UCSC Ensembl
Innerchr7:1127684..1158215hg18UCSC Ensembl
Innerchr7:934399..964930hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3830532
hg1930532
hg1830532
hg1730532
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522801
Supporting Variants
Samples
Known GenesC7orf50
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698446
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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