A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359483



Internal ID21017036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24581101..24587700hg38UCSC Ensembl
chr4:24582724..24589323hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211784
Samples
Known GenesDHX15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359483
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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