A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980895



Internal ID20547935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:54066884..54067367hg38UCSC Ensembl
chr10:55826644..55827127hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445725
Supporting Variants
Samples
Known GenesPCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer