A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967720



Internal ID18602948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3534242..3612477hg38UCSC Ensembl
Innerchr4:3535969..3614204hg19UCSC Ensembl
Innerchr4:3505767..3584002hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3878236
hg1978236
hg1878236
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2310601, nssv2310599, nssv2310596, nssv2310597, nssv2310600, nssv2310595, nssv2310594, nssv2310598, nssv2310602, nssv2310593
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00955
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967720
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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