A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636565



Internal ID7023359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55484284..55490748hg38UCSC Ensembl
Innerchr15:55484434..55490598hg38UCSC Ensembl
Outerchr15:55484134..55490898hg38UCSC Ensembl
chr15:55776482..55782946hg19UCSC Ensembl
Innerchr15:55776632..55782796hg19UCSC Ensembl
Outerchr15:55776332..55783096hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386465
hg196465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15256365
SamplesHG02253
Known GenesDYX1C1, DYX1C1-CCPG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636565
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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