A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132052



Internal ID20699092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37901890..37902356hg38UCSC Ensembl
chr5:37901992..37902458hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390132
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00086


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