A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634855



Internal ID7021655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70239299..70243170hg38UCSC Ensembl
chr14:70706016..70709887hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg383872
hg193872
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15052664, essv15052662, essv15052661, essv15052663
SamplesHG01694, NA18631, HG01105, HG01695
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634855
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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