A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062974



Internal ID18805505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50030442..50049637hg38UCSC Ensembl
Innerchr19:50533699..50552894hg19UCSC Ensembl
Innerchr19:55225511..55244706hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3819196
hg1919196
hg1819196
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3574991
Samples
Known GenesZNF473
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062974
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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