A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523431



Internal ID20896792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12740398..12749962hg38UCSC Ensembl
chr18:12740397..12749961hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg389565
hg199565
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190555
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523431
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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