A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503451



Internal ID20876706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25639769..25640377hg38UCSC Ensembl
chr16:25651090..25651698hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029541
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503451
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