A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553962



Internal ID16341371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31372513..31375622hg38UCSC Ensembl
Innerchr11:31394060..31397169hg19UCSC Ensembl
Innerchr11:31350636..31353745hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383110
hg193110
hg183110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1737n54
Supporting Variantsnssv770718, nssv770719, nssv770720, nssv770722, nssv770721
Samples
Known GenesDNAJC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553962
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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