A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521701



Internal ID15448994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6374338..6374568hg38UCSC Ensembl
Innerchr17:6277658..6277888hg19UCSC Ensembl
Innerchr17:6218382..6218612hg18UCSC Ensembl
Innerchr17:6218382..6218612hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38231
hg19231
hg18231
hg17231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694474
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521701
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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