A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5934668



Internal ID9661487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:115914724..115915634hg38UCSC Ensembl
chr12:116352529..116353439hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38911
hg19911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669405
Supporting Variants
SamplesNA19393
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5934668
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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