A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429786



Internal ID21087339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102928001..102929000hg38UCSC Ensembl
chr8:103940229..103941228hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162519
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429786
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