A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6107875



Internal ID9085278
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 Flag1
Merged StatusS
Merged Variantsesv2672524
Supporting Variants
SamplesNA19236
Known GenesGRIN2A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6107875
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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