A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639298



Internal ID7026081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80918206..80938218hg38UCSC Ensembl
chr16:80952103..80972115hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3820013
hg1920013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15535517, essv15535513, essv15535509, essv15535511, essv15535514, essv15535515, essv15535508, essv15535518, essv15535512, essv15535516, essv15535510
SamplesHG03455, NA19443, HG00335, HG01077, NA19452, NA20276, NA19037, NA19331, NA19324, HG03157, NA19351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639298
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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