A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524957



Internal ID20898318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3420340..3423812hg38UCSC Ensembl
chr18:3420338..3423810hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383473
hg193473
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189202
Samples
Known GenesTGIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524957
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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