A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214652



Internal ID20781693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174295078..174332994hg38UCSC Ensembl
chr4:175216229..175254145hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3837917
hg1937917
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379673
Supporting Variants
Samples
Known GenesCEP44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214652
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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