A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519902



Internal ID20893263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:1594535..1749538hg38UCSC Ensembl
chr18:1594536..1749539hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38155004
hg19155004
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3263n223
Supporting Variantsnssv18187110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519902
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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