A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637036



Internal ID7023830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81481333..81489239hg38UCSC Ensembl
Innerchr15:81481372..81489200hg38UCSC Ensembl
Outerchr15:81481294..81489278hg38UCSC Ensembl
chr15:81773674..81781580hg19UCSC Ensembl
Innerchr15:81773713..81781541hg19UCSC Ensembl
Outerchr15:81773635..81781619hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg387907
hg197907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15306761, essv15306760, essv15306759, essv15306762
SamplesNA20832, HG00308, HG01342, NA12154
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637036
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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