A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18131758



Internal ID20698798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5559449..5560854hg38UCSC Ensembl
chr5:5559562..5560967hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg381406
hg191406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391440
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18131758
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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