A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367152



Internal ID21024705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13158915..13165407hg38UCSC Ensembl
chr4:13160539..13167031hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg386493
hg196493
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210984
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367152
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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