A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634856



Internal ID7021656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70239390..70243323hg38UCSC Ensembl
Innerchr14:70239394..70243320hg38UCSC Ensembl
Outerchr14:70239387..70243327hg38UCSC Ensembl
chr14:70706107..70710040hg19UCSC Ensembl
Innerchr14:70706111..70710037hg19UCSC Ensembl
Outerchr14:70706104..70710044hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg383934
hg193934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv406e214
Supporting Variantsessv15052672, essv15052674, essv15052665, essv15052670, essv15052666, essv15052673, essv15052667, essv15052669, essv15052671, essv15052668
SamplesHG03687, HG03754, HG03722, HG03750, HG04017, HG03778, HG04026, HG03716, HG04056, HG04061
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634856
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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