A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962569



Internal ID18597812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25895385..26171864hg38UCSC Ensembl
Innerchr20:25876021..26152500hg19UCSC Ensembl
Innerchr20:25824021..26100500hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38276480
hg19276480
hg18276480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2233264, nssv2233268, nssv2233263, nssv2233260, nssv2233261, nssv2233262, nssv2233265, nssv2233266, nssv2233267, nssv2233269
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM182A, LOC100134868, NCOR1P1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962569
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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