A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928105



Internal ID22703340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43989877..44128613hg38UCSC Ensembl
chr15:44282075..44420811hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38138737
hg19138737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370232
Samples
Known GenesFRMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928105
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