A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084206



Internal ID21510171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23966687..23966847hg38UCSC Ensembl
chr14:24435896..24436056hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601508
Supporting Variants
SamplesNA24385
Known GenesDHRS4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084206
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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