A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842967



Internal ID22617902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35415928..35421027hg38UCSC Ensembl
chr5:35416030..35421129hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842967
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