A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635371



Internal ID7022170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93903372..93911862hg38UCSC Ensembl
Innerchr14:93903381..93911853hg38UCSC Ensembl
Outerchr14:93903363..93911871hg38UCSC Ensembl
chr14:94369718..94378208hg19UCSC Ensembl
Innerchr14:94369727..94378199hg19UCSC Ensembl
Outerchr14:94369709..94378217hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg388491
hg198491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15102293
SamplesHG01951
Known GenesFAM181A-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635371
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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