A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867416



Internal ID22642351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93541304..93546003hg38UCSC Ensembl
chr7:93170616..93175315hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509434
Samples
Known GenesCALCR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867416
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