A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677187



Internal ID9943292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61945681..61961287hg38UCSC Ensembl
chr16:61979585..61995191hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3815607
hg1915607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6268657, essv5840994
SamplesHG00692, NA18541
Known GenesCDH8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677187
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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