A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14959368



Internal ID1380660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32868336..32881768hg38UCSC Ensembl
Innerchr14:32868391..32881713hg38UCSC Ensembl
Outerchr14:32868281..32881823hg38UCSC Ensembl
chr14:33337542..33350974hg19UCSC Ensembl
Innerchr14:33337597..33350919hg19UCSC Ensembl
Outerchr14:33337487..33351029hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3813433
hg1913433
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633995
Supporting Variants
SamplesHG01250
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14959368
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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