A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042092



Internal ID20609132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48795459..48805744hg38UCSC Ensembl
chr18:46321830..46332115hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3810286
hg1910286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534485
Supporting Variants
Samples
Known GenesCTIF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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