A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751917



Internal ID18379477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16033738..16034258hg38UCSC Ensembl
Outerchr16:16033720..16034269hg38UCSC Ensembl
Innerchr16:16127595..16128115hg19UCSC Ensembl
Outerchr16:16127577..16128126hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553170
Supporting Variants
Samples
Known GenesABCC1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751917
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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