A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333393



Internal ID20866569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27670502..27677106hg38UCSC Ensembl
chr1:27997013..28003617hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg386605
hg196605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203515
Samples
Known GenesIFI6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333393
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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