A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003773



Internal ID21913116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81578633..81578976hg38UCSC Ensembl
chr8:82490868..82491211hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003773
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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