A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409556



Internal ID21067109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135267581..135327939hg38UCSC Ensembl
chr5:134603271..134663629hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3860359
hg1960359
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214489
Samples
Known GenesC5orf66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409556
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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