A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450538



Internal ID21108091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77187683..77198575hg38UCSC Ensembl
chr9:79802599..79813491hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3810893
hg1910893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188246
Samples
Known GenesVPS13A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450538
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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