A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382146



Internal ID21039699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57272910..57701197hg38UCSC Ensembl
chr4:58139076..58567363hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38428288
hg19428288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212548
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382146
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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