A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18123862



Internal ID20690903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:123055435..123056178hg38UCSC Ensembl
chr5:122391130..122391873hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413792
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18123862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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