A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375718



Internal ID21033271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8064415..8064754hg38UCSC Ensembl
chr5:8064528..8064867hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214216
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375718
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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