A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14655141



Internal ID5115793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18835522..18837141hg38UCSC Ensembl
Innerchr13:18835572..18837091hg38UCSC Ensembl
Outerchr13:18835472..18837191hg38UCSC Ensembl
chr13:19409662..19411281hg19UCSC Ensembl
Innerchr13:19409712..19411231hg19UCSC Ensembl
Outerchr13:19409612..19411331hg19UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg381620
hg191620
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3631364
Supporting Variants
SamplesNA18561
Known GenesANKRD20A9P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14655141
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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