A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412183



Internal ID21069736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90801225..90801626hg38UCSC Ensembl
chr5:90097042..90097443hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133754
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412183
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