A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965865



Internal ID18601095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23803466..23855906hg38UCSC Ensembl
Innerchr20:23784103..23836543hg19UCSC Ensembl
Innerchr20:23732103..23784543hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3852441
hg1952441
hg1852441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2232435, nssv2232438, nssv2232441, nssv2232432, nssv2232436, nssv2232437, nssv2232440, nssv2232434, nssv2232433, nssv2232439
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCST2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965865
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