A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636197



Internal ID7022993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38579090..38585172hg38UCSC Ensembl
Innerchr15:38579152..38585110hg38UCSC Ensembl
Outerchr15:38579028..38585234hg38UCSC Ensembl
chr15:38871291..38877373hg19UCSC Ensembl
Innerchr15:38871353..38877311hg19UCSC Ensembl
Outerchr15:38871229..38877435hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg386083
hg196083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15221224
SamplesHG03237
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636197
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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