A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219996



Internal ID20787036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85568099..85572646hg38UCSC Ensembl
chr9:88183014..88187561hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg384548
hg194548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447312
Supporting Variants
Samples
Known GenesAGTPBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219996
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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