A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047474



Internal ID20614514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29481946..29489508hg38UCSC Ensembl
chr19:29972853..29980415hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg387563
hg197563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530651
Supporting Variants
Samples
Known GenesLOC284395
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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