A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865989



Internal ID22640924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94067740..94073157hg38UCSC Ensembl
chr9:96830022..96835439hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385418
hg195418
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2166n209
Supporting Variantsnssv17514839, nssv17514840
Samples
Known GenesPTPDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865989
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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