A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980042



Internal ID20547082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32131428..32145047hg38UCSC Ensembl
chr10:32420356..32433975hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3813620
hg1913620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454655
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980042
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