A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400520



Internal ID21058073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107479451..107507238hg38UCSC Ensembl
chr5:106815152..106842939hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3827788
hg1927788
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212719
Samples
Known GenesEFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400520
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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