A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637289



Internal ID7024083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93345532..93448347hg38UCSC Ensembl
Innerchr15:93345682..93448197hg38UCSC Ensembl
Outerchr15:93345382..93448497hg38UCSC Ensembl
chr15:93888761..93991576hg19UCSC Ensembl
Innerchr15:93888911..93991426hg19UCSC Ensembl
Outerchr15:93888611..93991726hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38102816
hg19102816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15321861, essv15321862, essv15321860
SamplesNA20861, HG03888, HG03991
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637289
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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