A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18115652



Internal ID20682692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3323362..3333177hg38UCSC Ensembl
chr4:3325089..3334904hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg389816
hg199816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366280
Supporting Variants
Samples
Known GenesRGS12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18115652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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