A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965843



Internal ID18601073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2067251..2078638hg38UCSC Ensembl
Innerchr20:2047897..2059284hg19UCSC Ensembl
Innerchr20:1995897..2007284hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3811388
hg1911388
hg1811388
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2226996, nssv2226995, nssv2226989, nssv2226992, nssv2226991, nssv2226997, nssv2226998, nssv2226994, nssv2226990, nssv2226993
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)nsv965843
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer