A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972366



Internal ID18607582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62415164..62439954hg38UCSC Ensembl
Innerchr9:46726465..46751255hg19UCSC Ensembl
Innerchr9:46566461..46591251hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3824791
hg1924791
hg1824791
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2542518, nssv2542523, nssv2543316, nssv2543317, nssv2542522, nssv2542521, nssv2542516, nssv2542517, nssv2542520, nssv2542519
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKGFLP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972366
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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