A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979542



Internal ID20546582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118204193..118204851hg38UCSC Ensembl
chr10:119963705..119964363hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453300
Supporting Variants
Samples
Known GenesCASC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979542
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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