A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972053



Internal ID18260583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89300779..89374914hg38UCSC Ensembl
Innerchr11:89033947..89108082hg19UCSC Ensembl
Innerchr11:88673595..88747730hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3874136
hg1974136
hg1874136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1899183, nssv1899182, nssv1899184, nssv1899191, nssv1899188, nssv1899189, nssv1899187, nssv1899190, nssv1899185, nssv1899186
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNOX4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972053
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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