A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462411



Internal ID21119964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20443794..20453462hg38UCSC Ensembl
chr12:20596728..20606396hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg389669
hg199669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999931
Samples
Known GenesPDE3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462411
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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