A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972049



Internal ID18607265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:82798430..82807047hg38UCSC Ensembl
Innerchr11:82509472..82518089hg19UCSC Ensembl
Innerchr11:82187120..82195737hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg388618
hg198618
hg188618
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1898279, nssv1898276, nssv1898280, nssv1898277, nssv1898272, nssv1898275, nssv1898273, nssv1898281, nssv1898274, nssv1898278
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)nsv972049
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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