A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14869898



Internal ID2833563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97948411..97949795hg38UCSC Ensembl
Innerchr13:97948426..97949781hg38UCSC Ensembl
Outerchr13:97948397..97949810hg38UCSC Ensembl
chr13:98600665..98602049hg19UCSC Ensembl
Innerchr13:98600680..98602035hg19UCSC Ensembl
Outerchr13:98600651..98602064hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381385
hg191385
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633302
Supporting Variants
SamplesHG02497
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14869898
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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