A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15299959



Internal ID5301775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77200289..77219057hg38UCSC Ensembl
Innerchr15:77200292..77219055hg38UCSC Ensembl
Outerchr15:77200287..77219060hg38UCSC Ensembl
chr15:77492631..77511399hg19UCSC Ensembl
Innerchr15:77492634..77511397hg19UCSC Ensembl
Outerchr15:77492629..77511402hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3818769
hg1918769
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636958
Supporting Variants
SamplesHG02574
Known GenesPEAK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15299959
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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