A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636994



Internal ID6677101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78934166..78940717hg38UCSC Ensembl
Innerchr15:78934316..78940567hg38UCSC Ensembl
Outerchr15:78934016..78940867hg38UCSC Ensembl
chr15:79226508..79233059hg19UCSC Ensembl
Innerchr15:79226658..79232909hg19UCSC Ensembl
Outerchr15:79226358..79233209hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg386552
hg196552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15302771
SamplesNA19131
Known GenesCTSH
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636994
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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