A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6313496



Internal ID9290899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1747317..1765023hg38UCSC Ensembl
Outerchr19:1746946..1765393hg38UCSC Ensembl
Innerchr19:1747316..1765022hg19UCSC Ensembl
Outerchr19:1746945..1765392hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3818448
hg1918448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671081
Supporting Variants
SamplesHG01051
Known GenesONECUT3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6313496
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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