A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178762



Internal ID20745802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96260811..96265158hg38UCSC Ensembl
chr9:99023093..99027440hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg384348
hg194348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449069
Supporting Variants
Samples
Known GenesHSD17B3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178762
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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