A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981281



Internal ID20548321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28224161..28228676hg38UCSC Ensembl
chr10:28513090..28517605hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg384516
hg194516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450310
Supporting Variants
Samples
Known GenesMPP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981281
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