A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6491516



Internal ID9468919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5057249..5061484hg38UCSC Ensembl
chr16:5107250..5111485hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384236
hg194236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663484
Supporting Variants
SamplesHG00654
Known GenesC16orf89
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6491516
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