A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179176



Internal ID20746216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73484359..73484746hg38UCSC Ensembl
chr9:76099275..76099662hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440945
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00113


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