A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975156



Internal ID18610364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18209260..18224127hg38UCSC Ensembl
Innerchr11:18230807..18245674hg19UCSC Ensembl
Innerchr11:18187383..18202250hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3814868
hg1914868
hg1814868
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1877952, nssv1877960, nssv1877955, nssv1877959, nssv1877954, nssv1877961, nssv1877953, nssv1877957, nssv1877958, nssv1877956
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC494141
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975156
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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