A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133449



Internal ID20700489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79809050..79821450hg38UCSC Ensembl
chr5:79104873..79117273hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3812401
hg1912401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411642
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133449
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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