A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978015



Internal ID20545055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124627782..124634292hg38UCSC Ensembl
chr10:126316351..126322861hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386511
hg196511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438259
Supporting Variants
Samples
Known GenesFAM53B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978015
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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