A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5518550



Internal ID8910822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4084312..4091274hg38UCSC Ensembl
chr16:4134313..4141275hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386963
hg196963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672506
Supporting Variants
SamplesHG00375
Known GenesADCY9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5518550
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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