A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7758n223



Internal ID22810726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63291201..63395000hg38UCSC Ensembl
chr9:67246173..67349972hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38103800
hg19103800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6436635, nsv6454754, nsv6445493, nsv6443173, nsv6441063
Samples
Known GenesAQP7P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7758n223
Frequency
Sample Size19652
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer