A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15317178



Internal ID5318994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89845033..89856267hg38UCSC Ensembl
Innerchr15:89845033..89856267hg38UCSC Ensembl
Outerchr15:89844533..89856767hg38UCSC Ensembl
chr15:90388265..90399499hg19UCSC Ensembl
Innerchr15:90388265..90399499hg19UCSC Ensembl
Outerchr15:90387765..90399999hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3811235
hg1911235
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637203
Supporting Variants
SamplesHG04075
Known GenesAP3S2, C15orf38-AP3S2, MIR5094
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15317178
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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