A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965873



Internal ID18601103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34337914..34351115hg38UCSC Ensembl
Innerchr20:32925720..32938921hg19UCSC Ensembl
Innerchr20:32389381..32402582hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3813202
hg1913202
hg1813202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2235916, nssv2235911, nssv2235908, nssv2235915, nssv2235907, nssv2235914, nssv2235909, nssv2235912, nssv2235910, nssv2235913
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)nsv965873
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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