A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635093



Internal ID7021893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81665068..81708684hg38UCSC Ensembl
chr14:82131412..82175028hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3843617
hg1943617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv411e214
Supporting Variantsessv15080054
SamplesNA19713
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635093
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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