A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670780



Internal ID9936885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:77443724..77445737hg38UCSC Ensembl
Outerchr1:77443687..77445787hg38UCSC Ensembl
Innerchr1:77909409..77911422hg19UCSC Ensembl
Outerchr1:77909372..77911472hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg382101
hg192101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5512740
SamplesNA19725
Known GenesAK5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670780
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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