A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212110



Internal ID20779150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153337701..153349000hg38UCSC Ensembl
chr4:154258853..154270152hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3811300
hg1911300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389566
Supporting Variants
Samples
Known GenesMND1, TRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212110
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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