A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964034



Internal ID18599272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:27729328..27730788hg38UCSC Ensembl
Innerchr4:27730950..27732410hg19UCSC Ensembl
Innerchr4:27340048..27341508hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg381461
hg191461
hg181461
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2315378, nssv2315384, nssv2315381, nssv2315379, nssv2315382, nssv2315377, nssv2315383, nssv2315380, nssv2315386, nssv2315385
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)nsv964034
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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