A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405729



Internal ID21063282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119543997..119552678hg38UCSC Ensembl
chr5:118879692..118888373hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg388682
hg198682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212509
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405729
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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