A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203515



Internal ID20770555
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 StatusS
Merged Variantsnsv6333393
Supporting Variants
Samples
Known GenesIFI6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203515
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer