A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675159



Internal ID9941264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76591368..76723968hg38UCSC Ensembl
Outerchr2:76591334..76724003hg38UCSC Ensembl
Innerchr2:76818494..76951094hg19UCSC Ensembl
Outerchr2:76818460..76951129hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38132670
hg19132670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5826287
SamplesHG00672
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675159
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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