A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848328



Internal ID22623263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27254504..27256703hg38UCSC Ensembl
chr8:27112021..27114220hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508742
Samples
Known GenesSTMN4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848328
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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