A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524542



Internal ID20897903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3234264..3262127hg38UCSC Ensembl
chr20:3214910..3242773hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3827864
hg1927864
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203273
Samples
Known GenesC20orf194, SLC4A11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524542
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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