A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171796



Internal ID20738836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94427201..94428100hg38UCSC Ensembl
chr8:95439429..95440328hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415640
Supporting Variants
Samples
Known GenesFSBP, RAD54B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171796
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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