A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423917



Internal ID21081470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78243252..78294542hg38UCSC Ensembl
chr8:79155487..79206777hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3851291
hg1951291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423917
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