A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177432



Internal ID20744472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87298084..87304883hg38UCSC Ensembl
chr9:89912999..89919798hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438643
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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