A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419628



Internal ID21077181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61599401..61602800hg38UCSC Ensembl
chr8:62511960..62515359hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7365n223
Supporting Variantsnssv18168734
Samples
Known GenesASPH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419628
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