A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008692



Internal ID21918035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27835626..27835682hg38UCSC Ensembl
chr8:27693143..27693199hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568104
Samples
Known GenesPBK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008692
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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