A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752228



Internal ID18726474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57628865..57628933hg38UCSC Ensembl
chr16:57662777..57662845hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553481
Supporting Variants
Samples
Known GenesGPR56
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752228
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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