A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528889



Internal ID15456182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:76646332..76665972hg38UCSC Ensembl
Innerchr17:74642414..74662054hg19UCSC Ensembl
Innerchr17:72154009..72173649hg18UCSC Ensembl
Innerchr17:72154009..72173649hg17UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3819641
hg1919641
hg1819641
hg1719641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705573
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528889
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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