A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413887



Internal ID21071440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65857019..65899797hg38UCSC Ensembl
chr5:65152847..65195625hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3842779
hg1942779
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214831
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413887
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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