A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831729



Internal ID22606664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165429455..165432626hg38UCSC Ensembl
chr2:166285965..166289136hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg383172
hg193172
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831729
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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