A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672524



Internal ID9591943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9868144..9872631hg38UCSC Ensembl
Outerchr16:9868107..9872681hg38UCSC Ensembl
Innerchr16:9962001..9966488hg19UCSC Ensembl
Outerchr16:9961964..9966538hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg384575
hg194575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6107875
SamplesNA19236
Known GenesGRIN2A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672524
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