A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637186



Internal ID7023980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89058794..89067198hg38UCSC Ensembl
Innerchr15:89058794..89067198hg38UCSC Ensembl
Outerchr15:89058675..89067322hg38UCSC Ensembl
chr15:89602025..89610429hg19UCSC Ensembl
Innerchr15:89602025..89610429hg19UCSC Ensembl
Outerchr15:89601906..89610553hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg388405
hg198405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317063, essv15317064, essv15317065
SamplesNA12058, HG00129, HG03709
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637186
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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