A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15317189



Internal ID5319005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89908387..89909398hg38UCSC Ensembl
Innerchr15:89908400..89909386hg38UCSC Ensembl
Outerchr15:89908375..89909411hg38UCSC Ensembl
chr15:90451619..90452630hg19UCSC Ensembl
Innerchr15:90451632..90452618hg19UCSC Ensembl
Outerchr15:90451607..90452643hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381012
hg191012
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637206
Supporting Variants
SamplesNA20339
Known GenesC15orf38, C15orf38-AP3S2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15317189
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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