A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100401



Internal ID20667441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24000749..24010226hg38UCSC Ensembl
chr3:24042240..24051717hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg389478
hg199478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370386
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100401
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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