A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18079635



Internal ID20646675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164026353..164026736hg38UCSC Ensembl
chr2:164882863..164883246hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18079635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00097


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