A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961255



Internal ID18596501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58216170..58217445hg38UCSC Ensembl
Innerchr19:58727536..58728811hg19UCSC Ensembl
Innerchr19:63419348..63420623hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg381276
hg191276
hg181276
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2162315, nssv2162314, nssv2162311, nssv2162312, nssv2162318, nssv2162309, nssv2162316, nssv2162310, nssv2162313, nssv2162317
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)nsv961255
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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