A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576037



Internal ID16016760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:75724647..75733488hg38UCSC Ensembl
Innerchr17:73720727..73729569hg19UCSC Ensembl
Innerchr17:71232322..71241164hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg388842
hg198843
hg188843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5776n54
Supporting Variantsnssv876113
Samples
Known GenesITGB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576037
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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