A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042513



Internal ID20609553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55687462..55688138hg38UCSC Ensembl
chr18:53354693..53355369hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526519
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042513
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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