A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016743



Internal ID21926086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27710979..27711071hg38UCSC Ensembl
chr8:27568496..27568588hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016743
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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