A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186451



Internal ID20753491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43878739..44204566hg38UCSC Ensembl
chr15:44170937..44496764hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38325828
hg19325828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497929
Supporting Variants
Samples
Known GenesFRMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186451
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