A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963012



Internal ID18598254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14850272..14852860hg38UCSC Ensembl
Innerchr19:14961084..14963672hg19UCSC Ensembl
Innerchr19:14822084..14824672hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382589
hg192589
hg182589
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2136022, nssv2136027, nssv2136025, nssv2136031, nssv2136024, nssv2136026, nssv2136029, nssv2136030, nssv2136023, nssv2136028
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)nsv963012
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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