A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043669



Internal ID20610709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70002301..70039700hg38UCSC Ensembl
chr18:67669537..67706936hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3837400
hg1937400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524944
Supporting Variants
Samples
Known GenesRTTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043669
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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