A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579465



Internal ID16366874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:37377650..37426790hg38UCSC Ensembl
Innerchr19:37868552..37917692hg19UCSC Ensembl
Innerchr19:42560392..42609532hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3849141
hg1949141
hg1849141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899151
Samples
Known GenesZNF527, ZNF569
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579465
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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