A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042811



Internal ID20609851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71311750..71515826hg38UCSC Ensembl
chr18:68978986..69183062hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38204077
hg19204077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521103
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042811
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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