A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967008



Internal ID18602237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:42469594..42473171hg38UCSC Ensembl
Innerchr3:42511086..42514663hg19UCSC Ensembl
Innerchr3:42486090..42489667hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg383578
hg193578
hg183578
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2278170, nssv2278177, nssv2278172, nssv2278173, nssv2278171, nssv2278175, nssv2278178, nssv2278176, nssv2278169, nssv2278174
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)nsv967008
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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