A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659384



Internal ID9925490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4627539..4628138hg38UCSC Ensembl
chr16:4677540..4678139hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6156865, essv6399267, essv5957725, essv6215559, essv6574379, essv6184579, essv6219414, essv5877521, essv5492278, essv6504402, essv6311424, essv6226297, essv5530861, essv6402297
SamplesNA19394, NA12383, NA19393, NA20332, NA19190, NA18870, NA20806, NA19457, NA19904, NA19456, NA20127, HG00260, NA19321, NA19346
Known GenesMGRN1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659384
Frequency
Sample Size1151
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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