A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981200



Internal ID18616399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159525646..159526558hg38UCSC Ensembl
Innerchr6:159946678..159947590hg19UCSC Ensembl
Innerchr6:159866668..159867580hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38913
hg19913
hg18913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2429102, nssv2429096, nssv2429094, nssv2429097, nssv2429098, nssv2429103, nssv2429101, nssv2429100, nssv2429099, nssv2429095
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)nsv981200
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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