A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15279746



Internal ID5281562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68988427..68996644hg38UCSC Ensembl
Innerchr15:68988432..68996639hg38UCSC Ensembl
Outerchr15:68988422..68996649hg38UCSC Ensembl
chr15:69280766..69288983hg19UCSC Ensembl
Innerchr15:69280771..69288978hg19UCSC Ensembl
Outerchr15:69280761..69288988hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg388218
hg198218
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636816
Supporting Variants
SamplesHG02895
Known GenesMIR548H4, NOX5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15279746
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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