A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553982



Internal ID16341391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31374061..31375622hg38UCSC Ensembl
Innerchr11:31395608..31397169hg19UCSC Ensembl
Innerchr11:31352184..31353745hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381562
hg191562
hg181562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1739n54
Supporting Variantsnssv771040
Samples
Known GenesDNAJC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553982
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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