A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040631



Internal ID20607671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27309001..27312100hg38UCSC Ensembl
chr18:24888965..24892064hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040631
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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