A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496615



Internal ID20869818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57276046..57277732hg38UCSC Ensembl
chr16:57309958..57311644hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg381687
hg191687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029780
Samples
Known GenesPLLP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496615
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