A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964375



Internal ID18599613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:10999016..10999712hg38UCSC Ensembl
Innerchr20:10979664..10980360hg19UCSC Ensembl
Innerchr20:10927664..10928360hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38697
hg19697
hg18697
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2228988, nssv2228984, nssv2228992, nssv2228990, nssv2228989, nssv2228985, nssv2228987, nssv2228986, nssv2228991, nssv2228993
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)nsv964375
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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