A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607821



Internal ID21799868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72118931..72119021hg38UCSC Ensembl
chr14:72585648..72585738hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036314
Supporting Variants
Samples
Known GenesRGS6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607821
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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