A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831536



Internal ID22606471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142128788..142131737hg38UCSC Ensembl
chr2:142886357..142889306hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg382950
hg192950
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487714
Samples
Known GenesLRP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831536
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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