A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576034



Internal ID16016757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:75721290..75731974hg38UCSC Ensembl
Innerchr17:73717370..73728055hg19UCSC Ensembl
Innerchr17:71228965..71239650hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3810685
hg1910686
hg1810686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5775n54
Supporting Variantsnssv876109
Samples
Known GenesITGB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576034
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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