A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526533



Internal ID15453826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62973910..62983240hg38UCSC Ensembl
Innerchr17:61051271..61060601hg19UCSC Ensembl
Innerchr17:58405003..58414333hg18UCSC Ensembl
Innerchr17:58405003..58414333hg17UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg389331
hg199331
hg189331
hg179331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702846
Samples
Known GenesMIR548W
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526533
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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