A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849293



Internal ID22624228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34962235..34987830hg38UCSC Ensembl
chr8:34819753..34845348hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3825596
hg1925596
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509171
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849293
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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