A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103796



Internal ID20670836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72559383..72591623hg38UCSC Ensembl
chr3:72608534..72640774hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3832241
hg1932241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103796
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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