A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671884



Internal ID9591303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15465997..15470364hg38UCSC Ensembl
chr16:15559854..15564221hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg384368
hg194368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5492574, essv5717641, essv6137308
SamplesNA19461, NA19428, NA19440
Known GenesC16orf45
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671884
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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