A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527367



Internal ID15454660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46848125..46848182hg38UCSC Ensembl
Innerchr17:44925491..44925548hg19UCSC Ensembl
Innerchr17:42280490..42280547hg18UCSC Ensembl
Innerchr17:42280490..42280547hg17UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
hg1758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703798
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527367
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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