A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633804



Internal ID6673923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24274134..24318147hg38UCSC Ensembl
Innerchr14:24274207..24318074hg38UCSC Ensembl
Outerchr14:24274061..24318220hg38UCSC Ensembl
chr14:24743340..24787353hg19UCSC Ensembl
Innerchr14:24743413..24787280hg19UCSC Ensembl
Outerchr14:24743267..24787426hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3844014
hg1944014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14942276
SamplesHG00320
Known GenesCIDEB, DHRS1, LTB4R, LTB4R2, NOP9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633804
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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