A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836324



Internal ID22611259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50405994..50407401hg38UCSC Ensembl
chr3:50443425..50444832hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381408
hg191408
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493199, nssv17493200
Samples
Known GenesCACNA2D2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836324
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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