A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6232215



Internal ID9209618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89846945..89851628hg38UCSC Ensembl
chr15:90390177..90394860hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384684
hg194684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667255
Supporting Variants
SamplesNA18977
Known GenesAP3S2, C15orf38-AP3S2, MIR5094
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6232215
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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