A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578752



Internal ID16366161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18280264..18281832hg38UCSC Ensembl
Innerchr19:18391074..18392642hg19UCSC Ensembl
Innerchr19:18252074..18253642hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381569
hg191569
hg181569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6294n54
Supporting Variantsnssv895769, nssv895770
Samples
Known GenesJUND
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578752
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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