A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436198



Internal ID21093751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77823516..77833768hg38UCSC Ensembl
chr9:80438432..80448684hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3810253
hg1910253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196176
Samples
Known GenesGNAQ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436198
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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