A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981181



Internal ID18616380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121653579..121655510hg38UCSC Ensembl
Innerchr6:121974725..121976656hg19UCSC Ensembl
Innerchr6:122016424..122018355hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381932
hg191932
hg181932
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2422455, nssv2422460, nssv2422461, nssv2422463, nssv2422457, nssv2422462, nssv2422459, nssv2422458, nssv2422454, nssv2422456
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)nsv981181
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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