A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635463



Internal ID7022262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98474082..98575557hg38UCSC Ensembl
Innerchr14:98474105..98575534hg38UCSC Ensembl
Outerchr14:98474059..98575580hg38UCSC Ensembl
chr14:98940419..99041894hg19UCSC Ensembl
Innerchr14:98940442..99041871hg19UCSC Ensembl
Outerchr14:98940396..99041917hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38101476
hg19101476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv418e214
Supporting Variantsessv15106680
SamplesNA18628
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635463
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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