A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6278245



Internal ID9904361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:116168003..116183204hg38UCSC Ensembl
Outerchr3:116167966..116183254hg38UCSC Ensembl
Innerchr3:115886850..115902051hg19UCSC Ensembl
Outerchr3:115886813..115902101hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3815289
hg1915289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670807
Supporting Variants
SamplesNA20799
Known GenesLSAMP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6278245
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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