A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832271



Internal ID22607206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241800766..241802124hg38UCSC Ensembl
chr2:242740181..242741539hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381359
hg191359
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483465
Samples
Known GenesGAL3ST2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832271
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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