A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000968



Internal ID21910311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81069056..81110986hg38UCSC Ensembl
chr8:81981291..82023221hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3841931
hg1941931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582918
Samples
Known GenesPAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000968
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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