A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103025



Internal ID20670065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60587653..60953356hg38UCSC Ensembl
chr3:60573386..60939028hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38365704
hg19365643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368440
Supporting Variants
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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