A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903752



Internal ID22678922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60934021..61055961hg38UCSC Ensembl
chr3:60919693..61041633hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38121941
hg19121941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427558
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903752
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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