A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178009



Internal ID20745049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9202349..9203003hg38UCSC Ensembl
chr9:9202349..9203003hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424699
Supporting Variants
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00034


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