A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042732



Internal ID20609772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70286501..70289900hg38UCSC Ensembl
chr18:67953737..67957136hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528342
Supporting Variants
Samples
Known GenesSOCS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042732
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01057


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