A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180627



Internal ID20747667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49541401..49553000hg38UCSC Ensembl
chr15:49833598..49845197hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3811600
hg1911600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512883
Supporting Variants
Samples
Known GenesFAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180627
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00046


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