A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5856849



Internal ID9650451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221570610..221581083hg38UCSC Ensembl
chr1:221743952..221754425hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3810474
hg1910474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664927
Supporting Variants
SamplesNA19381
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5856849
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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