A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186560



Internal ID20753600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63775316..64080261hg38UCSC Ensembl
chr18:61442550..61747495hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38304946
hg19304946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520851
Supporting Variants
Samples
Known GenesHMSD, LINC00305, SERPINB10, SERPINB2, SERPINB7, SERPINB8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186560
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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