A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15302771



Internal ID5304587
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636994
Supporting Variants
SamplesNA19131
Known GenesCTSH
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15302771
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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