A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15372898



Internal ID5374714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10040904..10053088hg38UCSC Ensembl
chr16:10134761..10146945hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3812185
hg1912185
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637884
Supporting Variants
SamplesHG02763
Known GenesGRIN2A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15372898
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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