A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701764



Internal ID15091730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:63926450..63983358hg38UCSC Ensembl
Innerchr17:62003810..62060718hg19UCSC Ensembl
Innerchr17:59357542..59414450hg18UCSC Ensembl
Innerchr17:59357542..59414450hg17UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3856909
hg1956909
hg1856909
hg1756909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517272
Supporting Variants
Samples
Known GenesCD79B, SCN4A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701764
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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