A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919970



Internal ID22695193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31028067..31030899hg38UCSC Ensembl
chr9:31028065..31030897hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg382833
hg192833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445113
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919970
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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