A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975136



Internal ID18610344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96759..104869hg38UCSC Ensembl
Innerchr11:96759..104869hg19UCSC Ensembl
Innerchr11:86759..94869hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388111
hg198111
hg188111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2616660, nssv2616658, nssv2616656, nssv2616653, nssv2616654, nssv2616655, nssv2616659, nssv2616651, nssv2616657, nssv2616652
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975136
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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