A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390620



Internal ID21048173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28908301..28954500hg38UCSC Ensembl
chr5:28908408..28954607hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3846200
hg1946200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215785
Samples
Known GenesLSP1P3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390620
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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