A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18041926



Internal ID20608966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46751442..46758660hg38UCSC Ensembl
chr18:44331405..44338623hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg387219
hg197219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516554
Supporting Variants
Samples
Known GenesST8SIA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18041926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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