A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213572



Internal ID20780612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3901701..4299100hg38UCSC Ensembl
chr4:3903428..4300827hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38397400
hg19397400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375513
Supporting Variants
Samples
Known GenesFAM86EP, LYAR, OTOP1, TMEM128, ZBTB49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213572
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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