A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5412632



Internal ID191934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83854372..83854423hg38UCSC Ensembl
chr4:84775525..84775576hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5412632
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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