A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408700



Internal ID21066253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142672556..142699789hg38UCSC Ensembl
chr5:142052121..142079354hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3827234
hg1927234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213226
Samples
Known GenesFGF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408700
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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