A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963325



Internal ID18598566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62926387..62927086hg38UCSC Ensembl
Innerchr3:62912062..62912761hg19UCSC Ensembl
Innerchr3:62887102..62887801hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38700
hg19700
hg18700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2282126, nssv2282127, nssv2282124, nssv2282131, nssv2282125, nssv2282130, nssv2282129, nssv2282128, nssv2282123, nssv2282122
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)nsv963325
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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