A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212315



Internal ID20779355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59786721..61760277hg38UCSC Ensembl
chr3:59772447..61745951hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381973557
hg191973505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371677
Supporting Variants
Samples
Known GenesFHIT, PTPRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212315
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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