A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853272



Internal ID22628207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24072337..24079665hg38UCSC Ensembl
chr8:23929850..23937178hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg387329
hg197329
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853272
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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