A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516685



Internal ID20890046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5588564..5648375hg38UCSC Ensembl
chr20:5569210..5629021hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3859812
hg1959812
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203880
Samples
Known GenesGPCPD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516685
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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