A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043298



Internal ID20610338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61516893..61527855hg38UCSC Ensembl
chr18:59184126..59195088hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3810963
hg1910963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515695
Supporting Variants
Samples
Known GenesCDH20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043298
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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