A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981162



Internal ID18616361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:86081836..86105695hg38UCSC Ensembl
Innerchr6:86791554..86815413hg19UCSC Ensembl
Innerchr6:86848273..86872132hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3823860
hg1923860
hg1823860
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2416049, nssv2416055, nssv2416057, nssv2416050, nssv2416053, nssv2416051, nssv2416052, nssv2416056, nssv2416054, nssv2416048
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)nsv981162
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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