A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968660



Internal ID18603888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67622659..67670061hg38UCSC Ensembl
Innerchr9:46281131..46335906hg19UCSC Ensembl
Innerchr9:46171127..46225902hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3847403
hg1954776
hg1854776
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2541978, nssv2541974, nssv2541972, nssv2541973, nssv2541975, nssv2541971, nssv2541979, nssv2541980, nssv2541977, nssv2541976
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)nsv968660
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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