A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966261



Internal ID18601491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:37817841..37822301hg38UCSC Ensembl
Innerchr4:37819463..37823923hg19UCSC Ensembl
Innerchr4:37495858..37500318hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg384461
hg194461
hg184461
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2316519, nssv2316514, nssv2316516, nssv2316511, nssv2316515, nssv2316513, nssv2316517, nssv2316518, nssv2316512, nssv2316520
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)nsv966261
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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