A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126231



Internal ID20693271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:13576630..13582204hg38UCSC Ensembl
chr5:13576739..13582313hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg385575
hg195575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379191
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126231
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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