A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203256



Internal ID20770296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5460102..5719171hg38UCSC Ensembl
chr20:5440748..5699817hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38259070
hg19259070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534084
Supporting Variants
Samples
Known GenesGPCPD1, LINC00654, LOC643406
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203256
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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