A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962574



Internal ID18251131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34200236..34215468hg38UCSC Ensembl
Innerchr20:32788042..32803274hg19UCSC Ensembl
Innerchr20:32251703..32266935hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3815233
hg1915233
hg1815233
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2235705, nssv2235704, nssv2235711, nssv2235703, nssv2235710, nssv2235702, nssv2235706, nssv2235709, nssv2235707, nssv2235708
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)nsv962574
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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