A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968682



Internal ID18603910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63313037..63327330hg38UCSC Ensembl
Innerchr9:67268009..67282302hg19UCSC Ensembl
Innerchr9:66957829..66972122hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3814294
hg1914294
hg1814294
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2547276, nssv2547280, nssv2547277, nssv2547273, nssv2547278, nssv2547279, nssv2547271, nssv2547274, nssv2547272, nssv2547275
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)nsv968682
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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