A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961208



Internal ID18596454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34092527..34095779hg38UCSC Ensembl
Innerchr19:34583432..34586684hg19UCSC Ensembl
Innerchr19:39275272..39278524hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383253
hg193253
hg183253
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2145934, nssv2145933, nssv2145937, nssv2145935, nssv2145941, nssv2145939, nssv2145940, nssv2145936, nssv2145942, nssv2145938
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)nsv961208
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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