A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6079772



Internal ID9057175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3119358..3120987hg38UCSC Ensembl
chr19:3119356..3120985hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381630
hg191630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2669769
Supporting Variants
SamplesNA19711
Known GenesGNA11
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6079772
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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