A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390214



Internal ID21047767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:20667301..20867700hg38UCSC Ensembl
chr5:20667410..20867809hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38200400
hg19200400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390214
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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