A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970943



Internal ID18606165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134442219..134442914hg38UCSC Ensembl
Innerchr7:134126971..134127666hg19UCSC Ensembl
Innerchr7:133777511..133778206hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38696
hg19696
hg18696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2479469, nssv2479472, nssv2479470, nssv2479477, nssv2479475, nssv2479471, nssv2479468, nssv2479474, nssv2479476, nssv2479473
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAKR1B1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970943
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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