A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741798



Internal ID20517776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5728223..5729693hg38UCSC Ensembl
chr6:5728456..5729926hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381471
hg191471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272129
Samples
Known GenesFARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741798
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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