A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967810



Internal ID18256352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:165277344..165279814hg38UCSC Ensembl
Innerchr4:166198496..166200966hg19UCSC Ensembl
Innerchr4:166417946..166420416hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382471
hg192471
hg182471
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2340860, nssv2340858, nssv2340855, nssv2340854, nssv2340856, nssv2340863, nssv2340859, nssv2340861, nssv2340862, nssv2340857
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGK3P, KLHL2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967810
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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