A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965757



Internal ID18254301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:114082319..114086937hg38UCSC Ensembl
Innerchr6:114403483..114408101hg19UCSC Ensembl
Innerchr6:114510176..114514794hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384619
hg194619
hg184619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2421101, nssv2421104, nssv2421103, nssv2421100, nssv2421106, nssv2421107, nssv2421105, nssv2421098, nssv2421102, nssv2421099
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)nsv965757
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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