A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039894



Internal ID20606934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31129194..31137144hg38UCSC Ensembl
chr18:28709157..28717107hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg387951
hg197951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519821
Supporting Variants
Samples
Known GenesDSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039894
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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