A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895306



Internal ID22670387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60551483..60743752hg38UCSC Ensembl
chr3:60537216..60729485hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38192270
hg19192270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414361
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895306
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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