A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865352



Internal ID22640287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80086166..80094159hg38UCSC Ensembl
chr8:80998401..81006394hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg387994
hg197994
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509980
Samples
Known GenesTPD52
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865352
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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