A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671258



Internal ID9937363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:168815077..168815265hg38UCSC Ensembl
Outerchr1:168815040..168815315hg38UCSC Ensembl
Innerchr1:168784315..168784503hg19UCSC Ensembl
Outerchr1:168784278..168784553hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5631138
SamplesHG01101
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671258
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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