A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850850



Internal ID22625785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106770106..106771295hg38UCSC Ensembl
chr8:107782334..107783523hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504874
Samples
Known GenesABRA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850850
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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