A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981143



Internal ID18269656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:50912579..50924284hg38UCSC Ensembl
Innerchr6:50880292..50891997hg19UCSC Ensembl
Innerchr6:50988251..50999956hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3811706
hg1911706
hg1811706
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2410690, nssv2410691, nssv2410688, nssv2410689, nssv2410686, nssv2410685, nssv2410684, nssv2410692, nssv2410687, nssv2410693
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)nsv981143
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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