A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738224



Internal ID20514192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24878884..24879182hg38UCSC Ensembl
chr6:24879112..24879410hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283780
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738224
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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