A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18079357



Internal ID20646397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168543701..168546100hg38UCSC Ensembl
chr2:169400211..169402610hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342250
Supporting Variants
Samples
Known GenesCERS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18079357
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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