A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978844



Internal ID18614047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53085976..53086904hg38UCSC Ensembl
Innerchr19:53589229..53590157hg19UCSC Ensembl
Innerchr19:58281041..58281969hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38929
hg19929
hg18929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2157294, nssv2157288, nssv2157290, nssv2157291, nssv2157295, nssv2157297, nssv2157296, nssv2157292, nssv2157289, nssv2157293
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF160
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978844
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