A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267673



Internal ID20476891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186693364..186693692hg38UCSC Ensembl
chr4:187614518..187614846hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736477
Supporting Variants
Samples
Known GenesFAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267673
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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