A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042349



Internal ID20609389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58808420..58809238hg38UCSC Ensembl
chr18:56475652..56476470hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38819
hg19819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526023
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042349
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0015


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