A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583792



Internal ID21775835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83510310..83510434hg38UCSC Ensembl
chr8:84422545..84422669hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583792
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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