A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14686141



Internal ID5948001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32822366..32876071hg38UCSC Ensembl
chr13:33396504..33450209hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3853706
hg1953706
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3631730
Supporting Variants
SamplesNA19360
Known GenesLINC00423
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14686141
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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