A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637023



Internal ID7023817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80772535..80776670hg38UCSC Ensembl
Innerchr15:80772540..80776666hg38UCSC Ensembl
Outerchr15:80772531..80776675hg38UCSC Ensembl
chr15:81064876..81069011hg19UCSC Ensembl
Innerchr15:81064881..81069007hg19UCSC Ensembl
Outerchr15:81064872..81069016hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg384136
hg194136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv455e214
Supporting Variantsessv15305565
SamplesNA19056
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637023
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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