A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576038



Internal ID16016761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:75726149..75736192hg38UCSC Ensembl
Innerchr17:73722229..73732273hg19UCSC Ensembl
Innerchr17:71233824..71243868hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3810044
hg1910045
hg1810045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5777n54
Supporting Variantsnssv876114
Samples
Known GenesITGB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576038
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer