A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975951



Internal ID18611158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77729674..77735383hg38UCSC Ensembl
Innerchr11:77440719..77446428hg19UCSC Ensembl
Innerchr11:77118367..77124076hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg385710
hg195710
hg185710
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1895660, nssv1895657, nssv1895659, nssv1895654, nssv1895661, nssv1895655, nssv1895658, nssv1895656, nssv1895662, nssv1895663
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRSF1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975951
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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