A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15214189



Internal ID599061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35409903..35430253hg38UCSC Ensembl
chr15:35702104..35722454hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3820351
hg1920351
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636136
Supporting Variants
SamplesHG00262
Known GenesDPH6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15214189
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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