A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144493



Internal ID20711533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68967956..68968206hg38UCSC Ensembl
chr6:69677848..69678098hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411689
Supporting Variants
Samples
Known GenesBAI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144493
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00271


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