A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181257



Internal ID20748297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77909004..77909565hg38UCSC Ensembl
chr9:80523920..80524481hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437520
Supporting Variants
Samples
Known GenesGNAQ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181257
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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