A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484787



Internal ID21142340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109869319..109869789hg38UCSC Ensembl
chr12:110307124..110307594hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996886
Samples
Known GenesGLTP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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