A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848326



Internal ID22623261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92186427..92194425hg38UCSC Ensembl
chr8:93198655..93206653hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg387999
hg197999
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510243
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848326
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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