A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971986



Internal ID18607202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9604183..9607316hg38UCSC Ensembl
Innerchr11:9625730..9628863hg19UCSC Ensembl
Innerchr11:9582306..9585439hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383134
hg193134
hg183134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1874888, nssv1874889, nssv1874884, nssv1874887, nssv1874881, nssv1874885, nssv1874882, nssv1874880, nssv1874883, nssv1874886
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)nsv971986
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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