A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524486



Internal ID20897847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56415501..56421400hg38UCSC Ensembl
chr18:54082732..54088631hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189736
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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