A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512122



Internal ID20885452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53972988..53996862hg38UCSC Ensembl
chr16:54006900..54030774hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3823875
hg1923875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030115
Samples
Known GenesFTO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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