A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960790



Internal ID18249351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11799012..11804767hg38UCSC Ensembl
Innerchr19:11909827..11915582hg19UCSC Ensembl
Innerchr19:11770827..11776582hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385756
hg195756
hg185756
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2132656, nssv2132653, nssv2132660, nssv2132659, nssv2132655, nssv2132661, nssv2132658, nssv2132654, nssv2132657, nssv2132652
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF491
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960790
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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