A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828070



Internal ID22603005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161600299..161624511hg38UCSC Ensembl
chr1:161570089..161594301hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3824213
hg1924213
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467245, nssv17460561
Samples
Known GenesFCGR2C, FCGR3B, HSPA7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828070
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