A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963074



Internal ID18598316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53096412..53097876hg38UCSC Ensembl
Innerchr19:53599665..53601129hg19UCSC Ensembl
Innerchr19:58291477..58292941hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg381465
hg191465
hg181465
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2157393, nssv2157391, nssv2157394, nssv2157390, nssv2157389, nssv2157388, nssv2157385, nssv2157387, nssv2157386, nssv2157392
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)nsv963074
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