A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965149



Internal ID18600383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24096935..24098608hg38UCSC Ensembl
Innerchr3:24138426..24140099hg19UCSC Ensembl
Innerchr3:24113430..24115103hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381674
hg191674
hg181674
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2275121, nssv2275120, nssv2275124, nssv2275122, nssv2275115, nssv2275123, nssv2275119, nssv2275118, nssv2275117, nssv2275116
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)nsv965149
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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