A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211781



Internal ID20778821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24409942..24692090hg38UCSC Ensembl
chr4:24411565..24693713hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38282149
hg19282149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374451
Supporting Variants
Samples
Known GenesDHX15, MIR573
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211781
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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