A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961176



Internal ID18249736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9310928..9324286hg38UCSC Ensembl
Innerchr19:9421604..9434962hg19UCSC Ensembl
Innerchr19:9282604..9295962hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3813359
hg1913359
hg1813359
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2131827, nssv2131820, nssv2131824, nssv2131825, nssv2131828, nssv2131821, nssv2131829, nssv2131823, nssv2131822, nssv2131826
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesZNF559, ZNF559-ZNF177
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961176
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer