A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529282



Internal ID20902643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21876800..21881051hg38UCSC Ensembl
chr18:19456761..19461012hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg384252
hg194252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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