A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981108



Internal ID18616307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19342007..19351220hg38UCSC Ensembl
Innerchr6:19342238..19351451hg19UCSC Ensembl
Innerchr6:19450217..19459430hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg389214
hg199214
hg189214
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2395901, nssv2395907, nssv2395905, nssv2395161, nssv2395903, nssv2395902, nssv2395162, nssv2395906, nssv2395163, nssv2395904
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)nsv981108
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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