A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005514



Internal ID21914857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28881623..28881752hg38UCSC Ensembl
chr8:28739140..28739269hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567786
Samples
Known GenesINTS9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005514
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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