A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180940



Internal ID20747980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76837289..76886009hg38UCSC Ensembl
chr9:79452205..79500925hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3848721
hg1948721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445451
Supporting Variants
Samples
Known GenesPRUNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180940
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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