A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5958820



Internal ID8945744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:27672066..27676779hg38UCSC Ensembl
Outerchr3:27671909..27676932hg38UCSC Ensembl
Innerchr3:27713557..27718270hg19UCSC Ensembl
Outerchr3:27713400..27718423hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg385024
hg195024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662859
Supporting Variants
SamplesHG00476
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5958820
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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