A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520859



Internal ID15448152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34825635..34854070hg38UCSC Ensembl
Innerchr19:35316539..35344974hg19UCSC Ensembl
Innerchr19:40008379..40036814hg18UCSC Ensembl
Innerchr19:40008379..40036814hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3828436
hg1928436
hg1828436
hg1728436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681853, nssv676421
Samples
Known GenesLOC400685
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520859
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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