A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393694



Internal ID21051247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43712286..43825346hg38UCSC Ensembl
chr4:43714303..43827363hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38113061
hg19113061
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213663
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393694
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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