A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969360



Internal ID18604587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26671381..26687406hg38UCSC Ensembl
Innerchr6:26671609..26687634hg19UCSC Ensembl
Innerchr6:26779588..26795613hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3816026
hg1916026
hg1816026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv70n82
Supporting Variantsnssv2397570, nssv2397569, nssv2397563, nssv2397566, nssv2397567, nssv2397565, nssv2397564, nssv2397568, nssv2397561, nssv2397562
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)nsv969360
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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