A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699014



Internal ID15435666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:11158566..11433934hg38UCSC Ensembl
Innerchr7:11198193..11473561hg19UCSC Ensembl
Innerchr7:11164718..11440086hg18UCSC Ensembl
Innerchr7:10971433..11246801hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38275369
hg19275369
hg18275369
hg17275369
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523279
Supporting Variants
Samples
Known GenesPHF14, THSD7A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699014
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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