A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657907



Internal ID9924012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18455226..18455832hg38UCSC Ensembl
chr19:18566036..18566642hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5620194, essv5432096, essv5486082, essv6415877, essv5961084, essv6019060, essv5778302, essv6178783
SamplesHG00096, NA20512, HG01070, NA20317, NA12044, HG01048, NA19776, NA20754
Known GenesELL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657907
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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