A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964370



Internal ID18599608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1920719..1922529hg38UCSC Ensembl
Innerchr20:1901365..1903175hg19UCSC Ensembl
Innerchr20:1849365..1851175hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381811
hg191811
hg181811
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2228733, nssv2228729, nssv2228730, nssv2228736, nssv2228735, nssv2228731, nssv2228732, nssv2228738, nssv2228734, nssv2228737
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSIRPA
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964370
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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