A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046409



Internal ID20613449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42534101..42539400hg38UCSC Ensembl
chr19:43038253..43043552hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519711
Supporting Variants
Samples
Known GenesLIPE-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046409
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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