A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979412



Internal ID18614615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:6442873..6443717hg38UCSC Ensembl
Innerchr20:6423520..6424364hg19UCSC Ensembl
Innerchr20:6371520..6372364hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38845
hg19845
hg18845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2227994, nssv2227990, nssv2227987, nssv2227985, nssv2227986, nssv2227991, nssv2227988, nssv2227992, nssv2227989, nssv2227993
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)nsv979412
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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