A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575689



Internal ID16016412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:55837279..55887196hg38UCSC Ensembl
Innerchr17:53914640..53964557hg19UCSC Ensembl
Innerchr17:51269639..51319556hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3849918
hg1949918
hg1849918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv874122
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575689
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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