A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860154



Internal ID22635089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123752491..123755740hg38UCSC Ensembl
chr7:123392545..123395794hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg383250
hg193250
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500809
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860154
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