A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963317



Internal ID18598558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:51897860..51904323hg38UCSC Ensembl
Innerchr3:51931876..51938339hg19UCSC Ensembl
Innerchr3:51906916..51913379hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg386464
hg196464
hg186464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2280392, nssv2280385, nssv2280387, nssv2280391, nssv2280388, nssv2280393, nssv2280386, nssv2280390, nssv2280389, nssv2280394
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIQCF1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963317
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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