A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574372



Internal ID16361781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13233470..13252736hg38UCSC Ensembl
Innerchr17:13136787..13156053hg19UCSC Ensembl
Innerchr17:13077512..13096778hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3819267
hg1919267
hg1819267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866925
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574372
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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