A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092451



Internal ID20659492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102232703..102233600hg38UCSC Ensembl
chr3:101951547..101952444hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38898
hg19898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367945
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092451
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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