A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15321903



Internal ID4491326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93374350..93435024hg38UCSC Ensembl
chr15:93917579..93978253hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3860675
hg1960675
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637293
Supporting Variants
SamplesHG03991
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15321903
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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