A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635353



Internal ID7022152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93141406..93162229hg38UCSC Ensembl
Innerchr14:93141406..93162229hg38UCSC Ensembl
Outerchr14:93141111..93162520hg38UCSC Ensembl
chr14:93607751..93628574hg19UCSC Ensembl
Innerchr14:93607751..93628574hg19UCSC Ensembl
Outerchr14:93607456..93628865hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3820824
hg1920824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15098877
SamplesHG01680
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635353
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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