A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5671464



Internal ID9739024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82010102..82015982hg38UCSC Ensembl
chr16:82043707..82049587hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg385881
hg195881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660861
Supporting Variants
SamplesNA19675
Known GenesSDR42E1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5671464
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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