A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018969



Internal ID21928312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30245986..30246054hg38UCSC Ensembl
chr8:30103502..30103570hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558832
Samples
Known GenesMIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018969
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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