A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389512



Internal ID21047065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61484109..61507007hg38UCSC Ensembl
chr4:62349827..62372725hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3822899
hg1922899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210900
Samples
Known GenesLPHN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389512
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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