A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5856847



Internal ID8834250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9879442..9888353hg38UCSC Ensembl
Outerchr3:9879405..9888403hg38UCSC Ensembl
Innerchr3:9921126..9930037hg19UCSC Ensembl
Outerchr3:9921089..9930087hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg388999
hg198999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666111
Supporting Variants
SamplesNA18973
Known GenesCIDEC
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5856847
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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