A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229382



Internal ID20796422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97696371..97840954hg38UCSC Ensembl
chr9:100458653..100603236hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38144584
hg19144584
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436895
Supporting Variants
Samples
Known GenesXPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229382
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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