A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635096



Internal ID7021896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81727010..81728689hg38UCSC Ensembl
Innerchr14:81727160..81728539hg38UCSC Ensembl
Outerchr14:81726860..81728839hg38UCSC Ensembl
chr14:82193354..82195033hg19UCSC Ensembl
Innerchr14:82193504..82194883hg19UCSC Ensembl
Outerchr14:82193204..82195183hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg381680
hg191680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15080057
SamplesHG01807
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635096
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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