A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374451



Internal ID21032004
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 StatusM
Merged Variants
Supporting Variantsnssv18211781
Samples
Known GenesDHX15, MIR573
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374451
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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