A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972329



Internal ID18607545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66957536..67007226hg38UCSC Ensembl
Innerchr9:40685615..40735305hg19UCSC Ensembl
Innerchr9:40675615..40725305hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3849691
hg1949691
hg1849691
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2533741, nssv2533744, nssv2533737, nssv2533743, nssv2533746, nssv2533739, nssv2533738, nssv2533745, nssv2533740, nssv2533742
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM74A3, SPATA31A3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972329
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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