A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096691



Internal ID22005924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23939281..23939281hg38UCSC Ensembl
chr14:24408490..24408490hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602886
Samples
Known GenesDHRS4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096691
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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