A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406998



Internal ID21064551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161862033..161865620hg38UCSC Ensembl
chr5:161289039..161292626hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg383588
hg193588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126626
Samples
Known GenesGABRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406998
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