A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042940



Internal ID20609980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:53545394..53545462hg38UCSC Ensembl
chr18:51071764..51071832hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530717
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042940
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00855


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