A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845909



Internal ID22620844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1717272..1720095hg38UCSC Ensembl
chr7:1756908..1759731hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg382824
hg192824
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504078
Samples
Known GenesELFN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845909
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