A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969381



Internal ID18604608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32059838..32062525hg38UCSC Ensembl
Innerchr6:32027615..32030302hg19UCSC Ensembl
Innerchr6:32135593..32138280hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg382688
hg192688
hg182688
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2403352, nssv2403355, nssv2403353, nssv2403354, nssv2403359, nssv2403356, nssv2403360, nssv2403357, nssv2403351, nssv2403358
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTNXB
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969381
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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