A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968717



Internal ID18257259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87727978..87729326hg38UCSC Ensembl
Innerchr9:90342893..90344241hg19UCSC Ensembl
Innerchr9:89532713..89534061hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381349
hg191349
hg181349
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2556641, nssv2556648, nssv2556645, nssv2556642, nssv2556640, nssv2556649, nssv2556643, nssv2556644, nssv2556646, nssv2556647
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCTSL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968717
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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