A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14672871



Internal ID3132929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25033923..25035064hg38UCSC Ensembl
Innerchr13:25033968..25035019hg38UCSC Ensembl
Outerchr13:25033878..25035109hg38UCSC Ensembl
chr13:25608061..25609202hg19UCSC Ensembl
Innerchr13:25608106..25609157hg19UCSC Ensembl
Outerchr13:25608016..25609247hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381142
hg191142
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3631576
Supporting Variants
SamplesHG02760
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14672871
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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