A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635333



Internal ID7022132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92188696..92246996hg38UCSC Ensembl
Innerchr14:92188742..92246951hg38UCSC Ensembl
Outerchr14:92188651..92247042hg38UCSC Ensembl
chr14:92655040..92713340hg19UCSC Ensembl
Innerchr14:92655086..92713295hg19UCSC Ensembl
Outerchr14:92654995..92713386hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3858301
hg1958301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv416e214
Supporting Variantsessv15098028
SamplesHG03875
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635333
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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