A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236375



Internal ID20803415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9875732..10083197hg38UCSC Ensembl
chr9:9875732..10083197hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38207466
hg19207466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426150
Supporting Variants
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236375
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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