A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197000



Internal ID20764040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7999672..8020367hg38UCSC Ensembl
chr9:7999672..8020367hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3820696
hg1920696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419228
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197000
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00496


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