A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18120052



Internal ID20687092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7099271..7106743hg38UCSC Ensembl
chr4:7100998..7108470hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg387473
hg197473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360827
Supporting Variants
Samples
Known GenesFLJ36777
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18120052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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