A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975232



Internal ID18610440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119586171..119586671hg38UCSC Ensembl
Innerchr11:119456883..119457383hg19UCSC Ensembl
Innerchr11:118962093..118962593hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1906169, nssv1906172, nssv1906168, nssv1906173, nssv1906171, nssv1906174, nssv1906177, nssv1906175, nssv1906170, nssv1906176
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)nsv975232
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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