A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751794



Internal ID18379354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4828177..4829736hg38UCSC Ensembl
Outerchr16:4828133..4829837hg38UCSC Ensembl
Innerchr16:4878178..4879737hg19UCSC Ensembl
Outerchr16:4878134..4879838hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381705
hg191705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553047
Supporting Variants
Samples
Known GenesGLYR1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751794
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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