A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5765511



Internal ID8742914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:17381891..17385889hg38UCSC Ensembl
chr16:17475748..17479746hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg383999
hg193999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656946
Supporting Variants
SamplesNA18963
Known GenesXYLT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5765511
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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