A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143840



Internal ID20710880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68718907..68721748hg38UCSC Ensembl
chr6:69428799..69431640hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg382842
hg192842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413658
Supporting Variants
Samples
Known GenesBAI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143840
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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