A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662163



Internal ID9928268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:212123897..212128805hg38UCSC Ensembl
Outerchr1:212123740..212128958hg38UCSC Ensembl
Innerchr1:212297239..212302147hg19UCSC Ensembl
Outerchr1:212297082..212302300hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg385219
hg195219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5972049
SamplesHG01350
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662163
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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