A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532711



Internal ID20906072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:40641832..40656224hg38UCSC Ensembl
chr18:38221796..38236188hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3814393
hg1914393
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532711
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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