A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15103416



Internal ID6869459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95667950..95677082hg38UCSC Ensembl
Innerchr14:95667950..95677082hg38UCSC Ensembl
Outerchr14:95667450..95677582hg38UCSC Ensembl
chr14:96134287..96143419hg19UCSC Ensembl
Innerchr14:96134287..96143419hg19UCSC Ensembl
Outerchr14:96133787..96143919hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg389133
hg199133
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635405
Supporting Variants
SamplesNA21095
Known GenesTCL6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15103416
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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