A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459620



Internal ID21117173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72598260..72600473hg38UCSC Ensembl
chr11:72309304..72311517hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382214
hg192214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992793
Samples
Known GenesPDE2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459620
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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