A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972381



Internal ID18607597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63330148..63350216hg38UCSC Ensembl
Innerchr9:67285120..67305188hg19UCSC Ensembl
Innerchr9:66974940..66995008hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3820069
hg1920069
hg1820069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2547450, nssv2547455, nssv2547451, nssv2547457, nssv2547453, nssv2547456, nssv2547448, nssv2547454, nssv2547452, nssv2547449
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAQP7P1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972381
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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