A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972046



Internal ID18607262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:74918886..74921206hg38UCSC Ensembl
Innerchr11:74629931..74632251hg19UCSC Ensembl
Innerchr11:74307579..74309899hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382321
hg192321
hg182321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1895837, nssv1895843, nssv1895838, nssv1895844, nssv1895842, nssv1895840, nssv1895839, nssv1895846, nssv1895845, nssv1895841
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesXRRA1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972046
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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