A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6446262



Internal ID9423665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2831488..2837881hg38UCSC Ensembl
chr16:2881489..2887882hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386394
hg196394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663371
Supporting Variants
SamplesNA19382
Known GenesZG16B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6446262
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