A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182553



Internal ID20749593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65495301..65537900hg38UCSC Ensembl
chr15:65787639..65830238hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3842600
hg1942600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505965
Supporting Variants
Samples
Known GenesDPP8, PTPLAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182553
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