A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404686



Internal ID21062239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131812719..131813933hg38UCSC Ensembl
chr5:131148412..131149626hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215847
Samples
Known GenesLOC728637
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404686
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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