A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656723



Internal ID9922828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11878909..11882797hg38UCSC Ensembl
Outerchr2:11878875..11882832hg38UCSC Ensembl
Innerchr2:12019035..12022923hg19UCSC Ensembl
Outerchr2:12019001..12022958hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg383958
hg193958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv680e199
Supporting Variantsessv5595359
SamplesHG00280
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656723
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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