A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660203



Internal ID9579622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8732191..8733867hg38UCSC Ensembl
chr16:8826048..8827724hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5408178, essv6537532, essv5548263, essv6060533, essv6226094, essv6308600, essv5726082, essv5726295, essv5929295, essv5612323, essv6427926, essv5973827, essv6108170, essv5399102, essv5487094, essv5929901, essv6259730
SamplesNA18520, NA19904, NA19311, NA20294, NA18517, NA19461, NA20322, NA19908, NA20282, NA19380, NA19189, NA18486, NA18510, NA19901, NA19711, NA19452, NA19350
Known GenesABAT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660203
Frequency
Sample Size1151
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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