A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138408



Internal ID20705448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138885201..138886600hg38UCSC Ensembl
chr6:139206338..139207737hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619537
Supporting Variants
Samples
Known GenesECT2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138408
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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