A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967011



Internal ID18602240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:44844876..44847533hg38UCSC Ensembl
Innerchr3:44886368..44889025hg19UCSC Ensembl
Innerchr3:44861372..44864029hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382658
hg192658
hg182658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2279947, nssv2279950, nssv2279951, nssv2279956, nssv2279954, nssv2279948, nssv2279949, nssv2279955, nssv2279953, nssv2279952
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKIF15
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967011
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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