A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832079



Internal ID22607014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183175512..183176811hg38UCSC Ensembl
chr2:184040240..184041539hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488759, nssv17488760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832079
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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