A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964413



Internal ID18252965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57483981..57489084hg38UCSC Ensembl
Innerchr20:56059037..56064140hg19UCSC Ensembl
Innerchr20:55492443..55497546hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg385104
hg195104
hg185104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2241419, nssv2241426, nssv2241423, nssv2241425, nssv2241420, nssv2241421, nssv2241422, nssv2241424, nssv2241417, nssv2241418
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)nsv964413
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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