A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048769



Internal ID20615809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52261150..52564057hg38UCSC Ensembl
chr19:52764403..53067310hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38302908
hg19302908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518489
Supporting Variants
Samples
Known GenesMIR643, ZNF480, ZNF528, ZNF534, ZNF578, ZNF610, ZNF766, ZNF808, ZNF880
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048769
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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