A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854010



Internal ID22628945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94068140..94075057hg38UCSC Ensembl
chr9:96830422..96837339hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg386918
hg196918
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2166n209
Supporting Variantsnssv17514842, nssv17514841
Samples
Known GenesPTPDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854010
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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