A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832913



Internal ID22607848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24192544..24201761hg38UCSC Ensembl
chr2:24415413..24424630hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg389218
hg199218
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483476, nssv17483477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832913
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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