A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830037



Internal ID22604972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46127706..46133580hg38UCSC Ensembl
chr1:46593378..46599252hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg385875
hg195875
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463358
Samples
Known GenesPIK3R3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830037
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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