A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402094



Internal ID21059647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:63809933..63818730hg38UCSC Ensembl
chr5:63105760..63114557hg19UCSC Ensembl
Cytoband5q12.2
Allele length
AssemblyAllele length
hg388798
hg198798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131410
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402094
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