A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6176619



Internal ID9858075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108463945..108475700hg38UCSC Ensembl
chr12:108857722..108869477hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3811756
hg1911756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676279
Supporting Variants
SamplesNA20527
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6176619
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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