A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18130841



Internal ID20697881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:30826305..30831214hg38UCSC Ensembl
chr5:30826412..30831321hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg384910
hg194910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394570
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18130841
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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