A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043410



Internal ID20610450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63593388..63594136hg38UCSC Ensembl
chr18:61260622..61261370hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527310
Supporting Variants
Samples
Known GenesSERPINB13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043410
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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