A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042084



Internal ID20609124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48543177..48543528hg38UCSC Ensembl
chr18:46069548..46069899hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521219
Supporting Variants
Samples
Known GenesCTIF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042084
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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