A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5843327



Internal ID9669086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46189072..46195005hg38UCSC Ensembl
chr2:46416211..46422144hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg385934
hg195934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659406
Supporting Variants
SamplesNA19398
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5843327
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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