A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18124697



Internal ID20691737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120581894..120598710hg38UCSC Ensembl
chr5:119917589..119934405hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3816817
hg1916817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410533
Supporting Variants
Samples
Known GenesPRR16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18124697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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