A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442597



Internal ID21100150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77975779..77976646hg38UCSC Ensembl
chr9:80590695..80591562hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38868
hg19868
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225646
Samples
Known GenesGNAQ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442597
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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