A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407640



Internal ID21065193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51907221..51935702hg38UCSC Ensembl
chr5:51203055..51231536hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3828482
hg1928482
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407640
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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