A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271488



Internal ID20480706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96049481..96049553hg38UCSC Ensembl
chr14:96515818..96515890hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734886
Supporting Variants
Samples
Known GenesC14orf132
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271488
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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