A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983039



Internal ID18618233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71557595..71566578hg38UCSC Ensembl
Innerchr11:71268641..71277624hg19UCSC Ensembl
Innerchr11:70946289..70955272hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg388984
hg198984
hg188984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1894462, nssv1894461, nssv1894465, nssv1894469, nssv1894466, nssv1894468, nssv1894463, nssv1894470, nssv1894464, nssv1894467
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKRTAP5-10
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983039
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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