A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499679



Internal ID20872902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27225933..27226158hg38UCSC Ensembl
chr16:27237254..27237479hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029268
Samples
Known GenesNSMCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499679
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