A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631833



Internal ID7018642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39484146..39494551hg38UCSC Ensembl
Innerchr13:39484296..39494401hg38UCSC Ensembl
Outerchr13:39483996..39494701hg38UCSC Ensembl
chr13:40058283..40068688hg19UCSC Ensembl
Innerchr13:40058433..40068538hg19UCSC Ensembl
Outerchr13:40058133..40068838hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3810406
hg1910406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv327e214
Supporting Variantsessv14702942, essv14702943, essv14702944, essv14702941
SamplesNA19002, NA19084, NA18994, NA18965
Known GenesLHFP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631833
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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