A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501907



Internal ID20875146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42900058..42914112hg38UCSC Ensembl
chr15:43192256..43206310hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3814055
hg1914055
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180215
Samples
Known GenesTTBK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501907
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer