A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658775



Internal ID9924880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29547436..29547839hg38UCSC Ensembl
chr16:29558757..29559160hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6230740, essv6183056, essv6246160, essv5655704, essv5739441, essv6146633, essv5700817, essv6333014, essv5663526
SamplesNA19394, NA19359, NA19393, NA19372, NA19445, NA19391, NA19452, NA19428, NA19398
Known GenesLOC440354
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658775
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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