A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480387



Internal ID21137940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118166101..118169900hg38UCSC Ensembl
chr12:118603906..118607705hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997235
Samples
Known GenesTAOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480387
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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