A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18111034



Internal ID20678074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157593175..157593782hg38UCSC Ensembl
chr4:158514327..158514934hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383323
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18111034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00092


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