A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481574



Internal ID21139127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87628095..87666597hg38UCSC Ensembl
chr13:88280350..88318852hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3838503
hg1938503
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181700
Samples
Known GenesMIR4500HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481574
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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