A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970110



Internal ID18605334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33363534..33375145hg38UCSC Ensembl
Innerchr6:33331311..33342922hg19UCSC Ensembl
Innerchr6:33439289..33450900hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3811612
hg1911612
hg1811612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2403840, nssv2404374, nssv2404372, nssv2404373, nssv2403838, nssv2403842, nssv2403843, nssv2403841, nssv2403839, nssv2404375
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)nsv970110
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer