A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279569



Internal ID20488787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64329889..64330180hg38UCSC Ensembl
chr14:64796607..64796898hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740019
Supporting Variants
Samples
Known GenesESR2, MIR548AZ
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279569
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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