A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5677522



Internal ID9047418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12318668..12335798hg38UCSC Ensembl
chr16:12412525..12429655hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3817131
hg1917131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670274
Supporting Variants
SamplesHG00692
Known GenesSNX29
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5677522
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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