A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635408



Internal ID7022207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95929517..95936372hg38UCSC Ensembl
Innerchr14:95929536..95936354hg38UCSC Ensembl
Outerchr14:95929499..95936391hg38UCSC Ensembl
chr14:96395854..96402709hg19UCSC Ensembl
Innerchr14:96395873..96402691hg19UCSC Ensembl
Outerchr14:96395836..96402728hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg386856
hg196856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103419
SamplesHG01896
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635408
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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