A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832939



Internal ID22607874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31632862..31648754hg38UCSC Ensembl
chr2:31857931..31873823hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg3815893
hg1915893
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832939
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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