A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393278



Internal ID21050831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:66544001..66596700hg38UCSC Ensembl
chr4:67409719..67462418hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3852700
hg1952700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393278
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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