A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422316



Internal ID21079869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61446314..61446940hg38UCSC Ensembl
chr8:62358873..62359499hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168729
Samples
Known GenesCLVS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422316
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