A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960817



Internal ID18596064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23373635..23423856hg38UCSC Ensembl
Innerchr19:23556437..23606658hg19UCSC Ensembl
Innerchr19:23348277..23398498hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3850222
hg1950222
hg1850222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2141943, nssv2141946, nssv2141944, nssv2141940, nssv2141942, nssv2141938, nssv2141945, nssv2141947, nssv2141939, nssv2141941
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF91
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960817
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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