A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180891



Internal ID20747931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77330921..77331422hg38UCSC Ensembl
chr9:79945837..79946338hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445040
Supporting Variants
Samples
Known GenesVPS13A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00129


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