A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477893



Internal ID21135446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87668701..87687800hg38UCSC Ensembl
chr13:88320956..88340055hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3819100
hg1919100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196450
Samples
Known GenesMIR4500HG, SLITRK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477893
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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