A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526637



Internal ID20899998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22440952..22441540hg38UCSC Ensembl
chr18:20020915..20021503hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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