A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671486



Internal ID9937591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:67815839..67817080hg38UCSC Ensembl
Outerchr16:67815682..67817233hg38UCSC Ensembl
Innerchr16:67849742..67850983hg19UCSC Ensembl
Outerchr16:67849585..67851136hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381552
hg191552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv502e199
Supporting Variantsessv5521041, essv5910923
SamplesHG00501, NA18873
Known GenesTSNAXIP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671486
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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