A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635476



Internal ID7022275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99016072..99025640hg38UCSC Ensembl
Innerchr14:99016072..99025640hg38UCSC Ensembl
Outerchr14:99015572..99026140hg38UCSC Ensembl
chr14:99482409..99491977hg19UCSC Ensembl
Innerchr14:99482409..99491977hg19UCSC Ensembl
Outerchr14:99481909..99492477hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg389569
hg199569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15106781
SamplesHG01686
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635476
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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