A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531952



Internal ID20905313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3298580..3349521hg38UCSC Ensembl
chr18:3298578..3349519hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3850942
hg1950942
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531952
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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