A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965150



Internal ID18600384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:25746201..25751427hg38UCSC Ensembl
Innerchr3:25787692..25792918hg19UCSC Ensembl
Innerchr3:25762696..25767922hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg385227
hg195227
hg185227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2275579, nssv2275575, nssv2275581, nssv2275580, nssv2275582, nssv2275578, nssv2275574, nssv2275577, nssv2275576, nssv2275573
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNGLY1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965150
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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