A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5413314



Internal ID192607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149734910..149734961hg38UCSC Ensembl
chr4:150656062..150656113hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16958079
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5413314
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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