A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376461



Internal ID21034014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24437397..24454903hg38UCSC Ensembl
chr5:24437506..24455012hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg3817507
hg1917507
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376461
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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