A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451792



Internal ID21109345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77852901..77855800hg38UCSC Ensembl
chr9:80467817..80470716hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185085
Samples
Known GenesGNAQ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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