A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102057



Internal ID20669097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29380630..29381302hg38UCSC Ensembl
chr3:29422121..29422793hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371445
Supporting Variants
Samples
Known GenesRBMS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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