A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666878



Internal ID9932983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:43853937..43856319hg38UCSC Ensembl
Outerchr7:43853780..43856472hg38UCSC Ensembl
Innerchr7:43893536..43895918hg19UCSC Ensembl
Outerchr7:43893379..43896071hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382693
hg192693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6352502
SamplesNA18549
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666878
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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