A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6109479



Internal ID9086882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1612633..1613105hg38UCSC Ensembl
chr19:1612632..1613104hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667087
Supporting Variants
SamplesHG01055
Known GenesTCF3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6109479
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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