A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964043



Internal ID18599281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43586858..43587463hg38UCSC Ensembl
Innerchr4:43588875..43589480hg19UCSC Ensembl
Innerchr4:43283632..43284237hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38606
hg19606
hg18606
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2318086, nssv2318084, nssv2318089, nssv2318083, nssv2318082, nssv2318088, nssv2318090, nssv2318085, nssv2318087, nssv2318081
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)nsv964043
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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