A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058141



Internal ID19147360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12387780..12433760hg38UCSC Ensembl
Innerchr19:12498594..12544574hg19UCSC Ensembl
Innerchr19:12359594..12405574hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3845981
hg1945981
hg1845981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3431n100
Supporting Variantsnssv3564705
Samples
Known GenesZNF443, ZNF799
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058141
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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