A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376875



Internal ID21034428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33513987..33514540hg38UCSC Ensembl
chr5:33514092..33514645hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216213
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376875
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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