A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526144



Internal ID20899505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:51279037..51285310hg38UCSC Ensembl
chr18:48805407..48811680hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg386274
hg196274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526144
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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