A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913694



Internal ID22688910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1003182..1011593hg38UCSC Ensembl
chr9:1003182..1011593hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg388412
hg198412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438288
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913694
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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