A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430712



Internal ID21088265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80975184..80975446hg38UCSC Ensembl
chr8:81887419..81887681hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171289
Samples
Known GenesPAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430712
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