A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020462



Internal ID21929805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9940409..9942232hg38UCSC Ensembl
chr12:10093008..10094831hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381824
hg191824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613662
Samples
Known GenesLOC102467076
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020462
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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