A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218688



Internal ID20785728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96847001..96897400hg38UCSC Ensembl
chr9:99609283..99659682hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3850400
hg1950400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436144
Supporting Variants
Samples
Known GenesLOC100132781, ZNF782
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218688
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00074


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