A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039841



Internal ID20606882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3056359..3064649hg38UCSC Ensembl
chr18:3056357..3064647hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg388291
hg198291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522098
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039841
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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