A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831899



Internal ID22606834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160019667..160021916hg38UCSC Ensembl
chr2:160876178..160878427hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg382250
hg192250
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488252
Samples
Known GenesPLA2R1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831899
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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