A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389152



Internal ID21046705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163727140..163743020hg38UCSC Ensembl
chr4:164648292..164664172hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3815881
hg1915881
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213764
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389152
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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