A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366531



Internal ID21024084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60273483..60358109hg38UCSC Ensembl
chr3:60259212..60343841hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3884627
hg1984630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102994
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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