A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902592



Internal ID22677752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59832833..59970124hg38UCSC Ensembl
chr3:59818559..59955850hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38137292
hg19137292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419141
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902592
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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