A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204471



Internal ID20771511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:78853177..78878458hg38UCSC Ensembl
chr1:79318862..79344143hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3825282
hg1925282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323093
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204471
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