A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392277



Internal ID21049830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96863601..96873000hg38UCSC Ensembl
chr4:97784752..97794151hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg389400
hg199400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5379n223
Supporting Variantsnssv18214372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392277
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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