A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15098110



Internal ID6860269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92850932..92852615hg38UCSC Ensembl
Innerchr14:92850958..92852589hg38UCSC Ensembl
Outerchr14:92850906..92852641hg38UCSC Ensembl
chr14:93317277..93318960hg19UCSC Ensembl
Innerchr14:93317303..93318934hg19UCSC Ensembl
Outerchr14:93317251..93318986hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381684
hg191684
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635345
Supporting Variants
SamplesNA21091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15098110
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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