A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636245



Internal ID7023041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41568344..41568888hg38UCSC Ensembl
Innerchr15:41568348..41568885hg38UCSC Ensembl
Outerchr15:41568341..41568892hg38UCSC Ensembl
chr15:41860542..41861086hg19UCSC Ensembl
Innerchr15:41860546..41861083hg19UCSC Ensembl
Outerchr15:41860539..41861090hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15230574
SamplesNA20332
Known GenesTYRO3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636245
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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