A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190789



Internal ID20757829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11461601..11465700hg38UCSC Ensembl
chr10:11503600..11507699hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449364
Supporting Variants
Samples
Known GenesUSP6NL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190789
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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