A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5847190



Internal ID9553594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146770679..146773355hg38UCSC Ensembl
chr6:147091815..147094491hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg382677
hg192677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665277
Supporting Variants
SamplesNA19084
Known GenesADGB
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5847190
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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