A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905287



Internal ID22680472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118765685..118765767hg38UCSC Ensembl
chr4:119686840..119686922hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416031
Samples
Known GenesSEC24D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905287
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