A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181182



Internal ID20748222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100807424..100929726hg38UCSC Ensembl
chr15:101347629..101469931hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38122303
hg19122303
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495830
Supporting Variants
Samples
Known GenesALDH1A3, LRRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181182
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