A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473526



Internal ID22531419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64305371..64307270hg38UCSC Ensembl
chr15:64597570..64599469hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853215
Supporting Variants
Samples
Known GenesCSNK1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473526
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