A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18123398



Internal ID20690438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10479023..10484044hg38UCSC Ensembl
chr5:10479135..10484156hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg385022
hg195022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392590
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18123398
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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