A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696125



Internal ID15086091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8696386..8818290hg38UCSC Ensembl
Innerchr17:8599704..8721608hg19UCSC Ensembl
Innerchr17:8540429..8662333hg18UCSC Ensembl
Innerchr17:8540429..8662333hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38121905
hg19121905
hg18121905
hg17121905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518675
Supporting Variants
Samples
Known GenesCCDC42, MFSD6L, PIK3R6, SPDYE4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696125
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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