A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637206



Internal ID6677313
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317189, essv15317187, essv15317188
SamplesNA20339, NA19309, NA18909
Known GenesC15orf38, C15orf38-AP3S2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637206
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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