A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011514



Internal ID21920857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94392902..94394110hg38UCSC Ensembl
chr8:95405130..95406338hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381209
hg191209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578454
Samples
Known GenesRAD54B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011514
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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