A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460183



Internal ID21117736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92080940..92123296hg38UCSC Ensembl
chr12:92474716..92517072hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3842357
hg1942357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005739
Samples
Known GenesC12orf79
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460183
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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