A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972036



Internal ID18607252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60078272..60086204hg38UCSC Ensembl
Innerchr11:59845745..59853677hg19UCSC Ensembl
Innerchr11:59602321..59610253hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg387933
hg197933
hg187933
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1891133, nssv1891127, nssv1891125, nssv1891134, nssv1891132, nssv1891130, nssv1891129, nssv1891126, nssv1891128, nssv1891131
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972036
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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