A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977888



Internal ID20544928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114695459..114738832hg38UCSC Ensembl
chr10:116455218..116498591hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3843374
hg1943374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446455
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977888
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