A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704630



Internal ID21376906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33575746..33576069hg38UCSC Ensembl
chr9:33575744..33576067hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389004
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704630
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.132184


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