A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471757



Internal ID21129310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69685058..69688878hg38UCSC Ensembl
chr12:70078838..70082658hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg383821
hg193821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002512
Samples
Known GenesBEST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471757
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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