A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460792



Internal ID21118345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71908009..72118628hg38UCSC Ensembl
chr12:72301789..72512408hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38210620
hg19210620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002924
Samples
Known GenesTBC1D15, TPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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