A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039380



Internal ID21948723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20385986..20386090hg38UCSC Ensembl
chr12:20538920..20539024hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615704
Samples
Known GenesPDE3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039380
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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