A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673757



Internal ID9939862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84883485..84885202hg38UCSC Ensembl
Outerchr15:84883448..84885252hg38UCSC Ensembl
Innerchr15:85426716..85428433hg19UCSC Ensembl
Outerchr15:85426679..85428483hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381805
hg191805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6327353
SamplesNA19107
Known GenesSLC28A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673757
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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