A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929984



Internal ID22705244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74903545..74903622hg38UCSC Ensembl
chr15:75195886..75195963hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381692
Samples
Known GenesFAM219B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929984
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