A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058182



Internal ID19147401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57477028..57491006hg38UCSC Ensembl
Innerchr19:57988396..58002374hg19UCSC Ensembl
Innerchr19:62680208..62694186hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3813979
hg1913979
hg1813979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3684n100
Supporting Variantsnssv3726648
Samples
Known GenesZNF419, ZNF772
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058182
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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