A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405122



Internal ID21062675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:85621301..85638500hg38UCSC Ensembl
chr5:84917119..84934318hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3817200
hg1917200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214284
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405122
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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