A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978732



Internal ID20545772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14658662..14660876hg38UCSC Ensembl
chr10:14700661..14702875hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382215
hg192215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441126
Supporting Variants
Samples
Known GenesFAM107B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978732
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