A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024115



Internal ID21933458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93169525..93169662hg38UCSC Ensembl
chr12:93563301..93563438hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612156
Samples
Known GenesLOC643339
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024115
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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