A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522174



Internal ID20895535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38101459..38105282hg38UCSC Ensembl
chr18:35681423..35685246hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg383824
hg193824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040490
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522174
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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