A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576039



Internal ID16016762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:75726149..75736441hg38UCSC Ensembl
Innerchr17:73722229..73732522hg19UCSC Ensembl
Innerchr17:71233824..71244117hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3810293
hg1910294
hg1810294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5777n54
Supporting Variantsnssv876116, nssv876115
Samples
Known GenesITGB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576039
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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