A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035941



Internal ID20602981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46733801..46734700hg38UCSC Ensembl
chr17:44811167..44812066hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535295
Supporting Variants
Samples
Known GenesNSF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035941
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