A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531289



Internal ID20904650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70660989..70736382hg38UCSC Ensembl
chr18:68328225..68403618hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3875394
hg1975394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042751
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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