A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522183



Internal ID20895544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34450438..34466068hg38UCSC Ensembl
chr18:32030402..32046032hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3815631
hg1915631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179339
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522183
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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