A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972662



Internal ID18607878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34189114..34191780hg38UCSC Ensembl
Innerchr9:34189112..34191778hg19UCSC Ensembl
Innerchr9:34179112..34181778hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg382667
hg192667
hg182667
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2527394, nssv2527397, nssv2527395, nssv2527393, nssv2527396, nssv2527400, nssv2527398, nssv2527391, nssv2527392, nssv2527399
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesUBAP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972662
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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