A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183682



Internal ID20750722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39595984..39779925hg38UCSC Ensembl
chr15:39888185..40072126hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38183942
hg19183942
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512500
Supporting Variants
Samples
Known GenesFSIP1, THBS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183682
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