A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580740



Internal ID21529233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85344172..85344316hg38UCSC Ensembl
chr8:86256401..86256545hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139949
SamplesHG03371
Known GenesCA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580740
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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