A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575575



Internal ID16362984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53445827..53483508hg38UCSC Ensembl
Innerchr17:51523188..51560869hg19UCSC Ensembl
Innerchr17:48878187..48915868hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3837682
hg1937682
hg1837682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5695n54
Supporting Variantsnssv873559
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575575
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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