A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18111136



Internal ID20678176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158648390..158656751hg38UCSC Ensembl
chr4:159569542..159577903hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg388362
hg198362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380595
Supporting Variants
Samples
Known GenesRXFP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18111136
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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