A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048201



Internal ID20615241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44866228..44869335hg38UCSC Ensembl
chr19:45369485..45372592hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg383108
hg193108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523800
Supporting Variants
Samples
Known GenesPVRL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048201
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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