A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698795



Internal ID15435447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62978029..62995263hg38UCSC Ensembl
Innerchr17:61055390..61072624hg19UCSC Ensembl
Innerchr17:58409122..58426356hg18UCSC Ensembl
Innerchr17:58409122..58426356hg17UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3817235
hg1917235
hg1817235
hg1717235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523102
Supporting Variants
Samples
Known GenesMIR548W
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698795
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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