A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185989



Internal ID20753029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65528618..65530788hg38UCSC Ensembl
chr15:65820956..65823126hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382171
hg192171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500755
Supporting Variants
Samples
Known GenesPTPLAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185989
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