A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426297



Internal ID21083850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55458301..55463900hg38UCSC Ensembl
chr8:56370861..56376460hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169123
Samples
Known GenesXKR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426297
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