A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049161



Internal ID20616201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55236798..55237359hg38UCSC Ensembl
chr19:55748166..55748727hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535519
Supporting Variants
Samples
Known GenesPPP6R1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049161
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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