A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211851



Internal ID20778891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28718539..29071955hg38UCSC Ensembl
chr4:28720161..29073577hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38353417
hg19353417
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361626
Supporting Variants
Samples
Known GenesMIR4275
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211851
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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