A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182617



Internal ID20749657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113145865..113152189hg38UCSC Ensembl
chr13:113800179..113806503hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg386325
hg196325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487552
Supporting Variants
Samples
Known GenesF10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182617
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