A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901808



Internal ID22676961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40466431..40468693hg38UCSC Ensembl
chr6:40434170..40436432hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg382263
hg192263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436750
Samples
Known GenesLRFN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901808
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer