A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968668



Internal ID18603896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62547274..62592413hg38UCSC Ensembl
Innerchr9:46858575..46903714hg19UCSC Ensembl
Innerchr9:46698571..46743710hg18UCSC Ensembl
Cytoband9p11.1
Allele length
AssemblyAllele length
hg3845140
hg1945140
hg1845140
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2543299, nssv2543295, nssv2543296, nssv2543292, nssv2543294, nssv2543300, nssv2543293, nssv2543298, nssv2543301, nssv2543297
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)nsv968668
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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