A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972945



Internal ID18608161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9638876..9662703hg38UCSC Ensembl
Innerchr11:9660423..9684250hg19UCSC Ensembl
Innerchr11:9616999..9640826hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3823828
hg1923828
hg1823828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2757456, nssv2760097, nssv2758595
SamplesHGDP00665, HGDP00998, HGDP00778
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972945
Frequency
Sample Size10
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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