A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460457



Internal ID21118010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104130556..104132357hg38UCSC Ensembl
chr12:104524334..104526135hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995686
Samples
Known GenesNFYB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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