A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678276



Internal ID9944381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43176583..43178127hg38UCSC Ensembl
chr15:43468781..43470325hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg381545
hg191545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6013017, essv6026280, essv6454838, essv6185383, essv5717184, essv6140264, essv5414556
SamplesNA19332, NA19443, NA19457, NA19908, HG01375, NA19470, NA19900
Known GenesTMEM62
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678276
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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