A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14942631



Internal ID4549552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24675077..24693168hg38UCSC Ensembl
chr14:25144283..25162374hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3818092
hg1918092
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633811
Supporting Variants
SamplesHG04047
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14942631
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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