A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967096



Internal ID18602325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179646793..179651736hg38UCSC Ensembl
Innerchr3:179364581..179369524hg19UCSC Ensembl
Innerchr3:180847275..180852218hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg384944
hg194944
hg184944
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2305335, nssv2305334, nssv2305333, nssv2305329, nssv2305336, nssv2305338, nssv2305337, nssv2305330, nssv2305332, nssv2305331
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)nsv967096
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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