A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474314



Internal ID22532208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84991879..84993178hg38UCSC Ensembl
chr15:85535110..85536409hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865065
Supporting Variants
Samples
Known GenesPDE8A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474314
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