A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420634



Internal ID21078187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101987507..101988744hg38UCSC Ensembl
chr8:102999735..103000972hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381238
hg191238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162047
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420634
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