A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972666



Internal ID18261196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35125325..35162706hg38UCSC Ensembl
Innerchr9:35125322..35162703hg19UCSC Ensembl
Innerchr9:35115322..35152703hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3837382
hg1937382
hg1837382
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2527627, nssv2527628, nssv2527624, nssv2527623, nssv2527630, nssv2527625, nssv2527631, nssv2527626, nssv2527632, nssv2527629
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesUNC13B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972666
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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