A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214766



Internal ID20781806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87978552..87979361hg38UCSC Ensembl
chr4:88899704..88900513hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385456
Supporting Variants
Samples
Known GenesSPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214766
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00049


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