A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831708



Internal ID22606643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160855339..160857342hg38UCSC Ensembl
chr2:161711850..161713853hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg382004
hg192004
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831708
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