A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5411134



Internal ID190446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:235744045..235744096hg38UCSC Ensembl
chr2:236652689..236652740hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16928681
Samples
Known GenesAGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5411134
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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