A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671484



Internal ID9937589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119620889..119620971hg38UCSC Ensembl
chr1:120163512..120163594hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6211036, essv5809152
SamplesNA18916, NA19147
Known GenesZNF697
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671484
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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