A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021840



Internal ID21931183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:128084706..128087711hg38UCSC Ensembl
chr12:128569251..128572256hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg383006
hg193006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608212
Samples
Known GenesLOC100996679
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021840
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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