A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042272



Internal ID20609312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:57132984..57133339hg38UCSC Ensembl
chr18:54800215..54800570hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042272
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001


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