A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18147601



Internal ID20714641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98883261..98947398hg38UCSC Ensembl
chr6:99331137..99395274hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3864138
hg1964138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615236
Supporting Variants
Samples
Known GenesFBXL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18147601
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