A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636164



Internal ID6676273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36907124..37638725hg38UCSC Ensembl
Innerchr15:36907274..37638575hg38UCSC Ensembl
Outerchr15:36906974..37638875hg38UCSC Ensembl
chr15:37199325..37930926hg19UCSC Ensembl
Innerchr15:37199475..37930776hg19UCSC Ensembl
Outerchr15:37199175..37931076hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38731602
hg19731602
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15217020
SamplesHG00365
Known GenesMEIS2, MIR8063
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636164
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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