A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121260



Internal ID20688300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98282901..98284500hg38UCSC Ensembl
chr4:99204052..99205651hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382836
Supporting Variants
Samples
Known GenesRAP1GDS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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