A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979862



Internal ID18615063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:101456437..101458027hg38UCSC Ensembl
Innerchr3:101175281..101176871hg19UCSC Ensembl
Innerchr3:102657971..102659561hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg381591
hg191591
hg181591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2290489, nssv2290496, nssv2290490, nssv2290493, nssv2290494, nssv2290491, nssv2290498, nssv2290497, nssv2290495, nssv2290492
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSENP7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979862
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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