A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961209



Internal ID18596455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34127113..34127613hg38UCSC Ensembl
Innerchr19:34618018..34618518hg19UCSC Ensembl
Innerchr19:39309858..39310358hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2145033, nssv2145031, nssv2145038, nssv2145037, nssv2145030, nssv2145036, nssv2145035, nssv2145032, nssv2145029, nssv2145034
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)nsv961209
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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