A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194009



Internal ID20761049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99595090..99595788hg38UCSC Ensembl
chr9:102357372..102358070hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448454
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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