A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523102



Internal ID15450395
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 StatusM
Merged Variants
Supporting Variantsnssv698795
Samples
Known GenesMIR548W
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523102
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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