A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635087



Internal ID7021887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81426277..81429953hg38UCSC Ensembl
Innerchr14:81426277..81429953hg38UCSC Ensembl
Outerchr14:81426014..81430219hg38UCSC Ensembl
chr14:81892621..81896297hg19UCSC Ensembl
Innerchr14:81892621..81896297hg19UCSC Ensembl
Outerchr14:81892358..81896563hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg383677
hg193677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15080045
SamplesHG01119
Known GenesSTON2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635087
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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