A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15217027



Internal ID5218843
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636168
Supporting Variants
SamplesHG02086
Known GenesMEIS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15217027
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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