A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846904



Internal ID22621839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25529219..25530443hg38UCSC Ensembl
chr7:25568839..25570063hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg381225
hg191225
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504809
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846904
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