A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960769



Internal ID18596016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:690863..696895hg38UCSC Ensembl
Innerchr19:690863..696895hg19UCSC Ensembl
Innerchr19:641863..647895hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386033
hg196033
hg186033
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2127670, nssv2127669, nssv2127677, nssv2127673, nssv2127671, nssv2127676, nssv2127668, nssv2127675, nssv2127674, nssv2127672
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPRSS57
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960769
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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