A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752622



Internal ID18380182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88710469..88710603hg38UCSC Ensembl
Outerchr16:88710463..88710608hg38UCSC Ensembl
Innerchr16:88776877..88777011hg19UCSC Ensembl
Outerchr16:88776871..88777016hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553875
Supporting Variants
Samples
Known GenesCTU2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752622
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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