A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855620



Internal ID22630555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80087016..80088739hg38UCSC Ensembl
chr8:80999251..81000974hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381724
hg191724
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509982, nssv17509981
Samples
Known GenesTPD52
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855620
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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