A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751976



Internal ID18726222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23036464..23038099hg38UCSC Ensembl
Outerchr16:23036085..23038287hg38UCSC Ensembl
Innerchr16:23047785..23049420hg19UCSC Ensembl
Outerchr16:23047406..23049608hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg382203
hg192203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553229
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751976
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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