A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636168



Internal ID6676277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37004115..37004931hg38UCSC Ensembl
Innerchr15:37004122..37004924hg38UCSC Ensembl
Outerchr15:37004108..37004938hg38UCSC Ensembl
chr15:37296316..37297132hg19UCSC Ensembl
Innerchr15:37296323..37297125hg19UCSC Ensembl
Outerchr15:37296309..37297139hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15217027
SamplesHG02086
Known GenesMEIS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636168
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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