A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970145



Internal ID18605369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80369778..80381431hg38UCSC Ensembl
Innerchr6:81079495..81091148hg19UCSC Ensembl
Innerchr6:81136214..81147867hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3811654
hg1911654
hg1811654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2416682, nssv2416685, nssv2416677, nssv2416684, nssv2416681, nssv2416679, nssv2416678, nssv2416676, nssv2416683, nssv2416680
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)nsv970145
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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