A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409142



Internal ID21066695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146483820..146486058hg38UCSC Ensembl
chr5:145863383..145865621hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382239
hg192239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126048
Samples
Known GenesTCERG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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