A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5412101



Internal ID191405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161314334..161314385hg38UCSC Ensembl
chr2:162170845..162170896hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16920232
Samples
Known GenesPSMD14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5412101
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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