A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964031



Internal ID18599269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9627825..9763331hg38UCSC Ensembl
Innerchr4:9629449..9764955hg19UCSC Ensembl
Innerchr4:9238547..9374053hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38135507
hg19135507
hg18135507
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2313102, nssv2313108, nssv2313100, nssv2313103, nssv2313109, nssv2313106, nssv2313107, nssv2313104, nssv2313105, nssv2313101
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)nsv964031
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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