A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968744



Internal ID18603972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107167575..107170748hg38UCSC Ensembl
Innerchr9:109929856..109933029hg19UCSC Ensembl
Innerchr9:108969677..108972850hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg383174
hg193174
hg183174
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2564718, nssv2564717, nssv2564722, nssv2564725, nssv2564726, nssv2564723, nssv2564720, nssv2564724, nssv2564719, nssv2564721
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968744
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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