A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862440



Internal ID22637375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149691280..149693882hg38UCSC Ensembl
chr7:149388371..149390973hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg382603
hg192603
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862440
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