A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406069



Internal ID21063622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145311201..145333700hg38UCSC Ensembl
chr5:144690764..144713263hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3822500
hg1922500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406069
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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