A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978841



Internal ID18267358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52479804..52584984hg38UCSC Ensembl
Innerchr19:52983057..53088237hg19UCSC Ensembl
Innerchr19:57674869..57780049hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38105181
hg19105181
hg18105181
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2156157, nssv2156158, nssv2156162, nssv2156156, nssv2156154, nssv2156160, nssv2156155, nssv2156161, nssv2156159, nssv2156153
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF578, ZNF701, ZNF808
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978841
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