A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18041483



Internal ID20608523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5152666..5190794hg38UCSC Ensembl
chr18:5152665..5190793hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3838129
hg1938129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532416
Supporting Variants
Samples
Known GenesC18orf42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18041483
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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