A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963370



Internal ID18598611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:160076458..160080716hg38UCSC Ensembl
Innerchr3:159794245..159798503hg19UCSC Ensembl
Innerchr3:161276939..161281197hg18UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg384259
hg194259
hg184259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2302436, nssv2302434, nssv2302440, nssv2302437, nssv2302441, nssv2302438, nssv2302439, nssv2302433, nssv2302442, nssv2302435
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIL12A-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963370
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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