A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975235



Internal ID18610443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:123047706..123050310hg38UCSC Ensembl
Innerchr11:122918414..122921018hg19UCSC Ensembl
Innerchr11:122423624..122426228hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382605
hg192605
hg182605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1908321, nssv1908329, nssv1908324, nssv1908328, nssv1908323, nssv1908326, nssv1908327, nssv1908325, nssv1908330, nssv1908322
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)nsv975235
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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