A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119026



Internal ID20686066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69742608..69743773hg38UCSC Ensembl
chr4:70608326..70609491hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385364
Supporting Variants
Samples
Known GenesSULT1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119026
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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