A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020306



Internal ID21929649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74497937..74498025hg38UCSC Ensembl
chr8:75410172..75410260hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020306
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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