A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732605



Internal ID20508529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6117675..6117787hg38UCSC Ensembl
chr20:6098322..6098434hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268889
Samples
Known GenesFERMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732605
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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