A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968727



Internal ID18603955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90731930..90752459hg38UCSC Ensembl
Innerchr9:93494212..93514741hg19UCSC Ensembl
Innerchr9:92534032..92554562hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3820530
hg1920530
hg1820531
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2556957, nssv2556963, nssv2556962, nssv2556961, nssv2556960, nssv2556965, nssv2556958, nssv2556956, nssv2556959, nssv2556964
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)nsv968727
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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