A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193161



Internal ID20760201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9367332..9398574hg38UCSC Ensembl
chr10:9409295..9440537hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3831243
hg1931243
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193161
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