A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646992



Internal ID21595297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23939284..23939284hg38UCSC Ensembl
chr14:24408493..24408493hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089708
SamplesHG00731
Known GenesDHRS4-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646992
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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