A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526073



Internal ID15453366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:71108203..71109443hg38UCSC Ensembl
Innerchr17:69104344..69105584hg19UCSC Ensembl
Innerchr17:66615939..66617179hg18UCSC Ensembl
Innerchr17:66615939..66617179hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381241
hg191241
hg181241
hg171241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702313
Samples
Known GenesCASC17
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526073
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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