A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407886



Internal ID21065439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73448601..73454800hg38UCSC Ensembl
chr5:72744426..72750625hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407886
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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