A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832456



Internal ID22607391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:217311782..217318084hg38UCSC Ensembl
chr2:218176505..218182807hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg386303
hg196303
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482654
Samples
Known GenesDIRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832456
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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