A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659334



Internal ID9925439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79491611..79641774hg38UCSC Ensembl
chr1:79957296..80107459hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38150164
hg19150164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6084551, essv6143122
SamplesHG00106, HG01048
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659334
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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