A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026476



Internal ID21935819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124912055..124912281hg38UCSC Ensembl
chr12:125396601..125396827hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609724
Samples
Known GenesUBC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026476
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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