A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963315



Internal ID18598556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:45155221..45160793hg38UCSC Ensembl
Innerchr3:45196713..45202285hg19UCSC Ensembl
Innerchr3:45171717..45177289hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg385573
hg195573
hg185573
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2280143, nssv2280144, nssv2280145, nssv2280142, nssv2280942, nssv2280146, nssv2280141, nssv2280941, nssv2280940, nssv2280147
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)nsv963315
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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