A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501758



Internal ID20874995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39779601..39783000hg38UCSC Ensembl
chr15:40071802..40075201hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190725
Samples
Known GenesFSIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501758
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