A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092315



Internal ID20659356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104059500..104060218hg38UCSC Ensembl
chr3:103778344..103779062hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356510
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092315
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00046


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