A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637203



Internal ID6677310
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317179, essv15317178
SamplesNA18977, HG04075
Known GenesAP3S2, C15orf38-AP3S2, MIR5094
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637203
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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