A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666642



Internal ID9932747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12013039..12013548hg38UCSC Ensembl
chr16:12106896..12107405hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6103526, essv6081080, essv5886601, essv5561961, essv5626389
SamplesNA19058, NA18545, HG00525, NA18559, HG00580
Known GenesSNX29
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666642
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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