A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197064



Internal ID20764104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83948478..83968795hg38UCSC Ensembl
chr15:84617230..84637547hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3820318
hg1920318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501471
Supporting Variants
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197064
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