A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039998



Internal ID20607038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32837905..32838412hg38UCSC Ensembl
chr18:30417868..30418375hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531542
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00074


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