A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381439



Internal ID21038992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5974010..5977045hg38UCSC Ensembl
chr5:5974123..5977158hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg383036
hg193036
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381439
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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