A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389124



Internal ID21046677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10353001..10354400hg38UCSC Ensembl
chr5:10353113..10354512hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212611
Samples
Known GenesMARCH6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389124
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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