A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101071



Internal ID20668111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24811096..24811696hg38UCSC Ensembl
chr3:24852587..24853187hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360660
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00058


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