A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5504958



Internal ID8482361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31155108..31158939hg38UCSC Ensembl
Outerchr15:31155071..31158989hg38UCSC Ensembl
Innerchr15:31447311..31451142hg19UCSC Ensembl
Outerchr15:31447274..31451192hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg383919
hg193919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658003
Supporting Variants
SamplesNA19788
Known GenesTRPM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5504958
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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