A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972804



Internal ID18261334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122615207..122615707hg38UCSC Ensembl
Innerchr9:125377486..125377986hg19UCSC Ensembl
Innerchr9:124417307..124417807hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2566444, nssv2566448, nssv2566447, nssv2566449, nssv2566446, nssv2566443, nssv2566451, nssv2566442, nssv2566450, nssv2566445
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR1Q1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972804
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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