A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982987



Internal ID18618181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:16481270..16484491hg38UCSC Ensembl
Innerchr11:16502817..16506038hg19UCSC Ensembl
Innerchr11:16459393..16462614hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg383222
hg193222
hg183222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1877068, nssv1877073, nssv1877070, nssv1877069, nssv1877072, nssv1877071, nssv1877076, nssv1877075, nssv1877074, nssv1877077
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)nsv982987
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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