A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522407



Internal ID20895768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:65663414..65713062hg38UCSC Ensembl
chr18:63330650..63380298hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3849649
hg1949649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522407
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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