A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831405



Internal ID22606340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162230163..162237377hg38UCSC Ensembl
chr2:163086673..163093887hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg387215
hg197215
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488282
Samples
Known GenesFAP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831405
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer