A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190227



Internal ID20757267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125886501..125904400hg38UCSC Ensembl
chr10:127575070..127592969hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3817900
hg1917900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453312
Supporting Variants
Samples
Known GenesFANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190227
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.49001


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