A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979884



Internal ID18615085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141522332..141522966hg38UCSC Ensembl
Innerchr3:141241174..141241808hg19UCSC Ensembl
Innerchr3:142723864..142724498hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38635
hg19635
hg18635
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2297522, nssv2297526, nssv2297530, nssv2297528, nssv2297521, nssv2297527, nssv2297525, nssv2297523, nssv2297524, nssv2297529
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRASA2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979884
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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