A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960791



Internal ID18249352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11814567..11978299hg38UCSC Ensembl
Innerchr19:11925382..12089114hg19UCSC Ensembl
Innerchr19:11786382..11950114hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38163733
hg19163733
hg18163733
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2132753, nssv2132749, nssv2132754, nssv2132756, nssv2132750, nssv2132752, nssv2132757, nssv2132758, nssv2132751, nssv2132755
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesZNF439, ZNF440, ZNF69, ZNF700, ZNF763
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960791
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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