A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388787



Internal ID21046340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127727101..127737500hg38UCSC Ensembl
chr4:128648256..128658655hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210294
Samples
Known GenesSLC25A31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388787
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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