A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981361



Internal ID20548401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29606864..29608648hg38UCSC Ensembl
chr10:29895793..29897577hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381785
hg191785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443080
Supporting Variants
Samples
Known GenesSVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981361
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