A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660185



Internal ID9926290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165920796..165921489hg38UCSC Ensembl
chr1:165890033..165890726hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6571314, essv6147068, essv5825312, essv5483515, essv5500875, essv5998066
SamplesNA19704, NA19355, NA19382, NA19311, NA19463, NA18522
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660185
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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