A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039890



Internal ID20606930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31097147..31097940hg38UCSC Ensembl
chr18:28677110..28677903hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523675
Supporting Variants
Samples
Known GenesDSC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00844


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