A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633886



Internal ID7020690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27626001..27734978hg38UCSC Ensembl
Innerchr14:27626001..27734978hg38UCSC Ensembl
Outerchr14:27625501..27735478hg38UCSC Ensembl
chr14:28095207..28204184hg19UCSC Ensembl
Innerchr14:28095207..28204184hg19UCSC Ensembl
Outerchr14:28094707..28204684hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38108978
hg19108978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14947498
SamplesHG02628
Known GenesLINC00645
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633886
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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