A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536918



Internal ID312324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23939284..23939284hg38UCSC Ensembl
chr14:24408493..24408493hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693407
Samples
Known GenesDHRS4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536918
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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