A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908065



Internal ID22683275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:72199839..72199972hg38UCSC Ensembl
chr8:73112074..73112207hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908065
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