A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15093362



Internal ID660703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90581572..90583507hg38UCSC Ensembl
Innerchr14:90581593..90583486hg38UCSC Ensembl
Outerchr14:90581551..90583528hg38UCSC Ensembl
chr14:91047916..91049851hg19UCSC Ensembl
Innerchr14:91047937..91049830hg19UCSC Ensembl
Outerchr14:91047895..91049872hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg381936
hg191936
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635316
Supporting Variants
SamplesHG00306
Known GenesTTC7B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15093362
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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