A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751835



Internal ID18379395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8681270..8681875hg38UCSC Ensembl
Outerchr16:8681238..8681900hg38UCSC Ensembl
Innerchr16:8775127..8775732hg19UCSC Ensembl
Outerchr16:8775095..8775757hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553088
Supporting Variants
Samples
Known GenesABAT
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751835
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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