A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832311



Internal ID22607246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:187365987..187375299hg38UCSC Ensembl
chr2:188230714..188240026hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg389313
hg199313
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488799, nssv17481334
Samples
Known GenesCALCRL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832311
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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