A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915985



Internal ID22691204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124894913..124895830hg38UCSC Ensembl
chr9:127657192..127658109hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2191n209
Supporting Variantsnssv17439489
Samples
Known GenesGOLGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915985
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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