A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524332



Internal ID20897693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33029253..33070107hg38UCSC Ensembl
chr20:31617059..31657913hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3840855
hg1940855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203282
Samples
Known GenesBPIFB3, BPIFB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524332
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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