A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968689



Internal ID18603917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63542265..63698927hg38UCSC Ensembl
Innerchr9:68137999..68294661hg19UCSC Ensembl
Innerchr9:67627758..67784481hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38156663
hg19156663
hg18156724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2548879, nssv2548876, nssv2548878, nssv2548873, nssv2548880, nssv2548874, nssv2548875, nssv2548877, nssv2548882, nssv2548881
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)nsv968689
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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