A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392555



Internal ID21050108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40234438..40307495hg38UCSC Ensembl
chr4:40236058..40309512hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3873058
hg1973455
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213610
Samples
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392555
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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