A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283780



Internal ID20492998
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 StatusS
Merged Variantsnsv4738224
Supporting Variants
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283780
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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