A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197081



Internal ID20764121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96508131..96510775hg38UCSC Ensembl
chr9:99270413..99273057hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg382645
hg192645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454195
Supporting Variants
Samples
Known GenesCDC14B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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