A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220185



Internal ID20787225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87595140..87596981hg38UCSC Ensembl
chr9:90210055..90211896hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381842
hg191842
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446684
Supporting Variants
Samples
Known GenesDAPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220185
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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