A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668729



Internal ID9588148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59550320..59641606hg38UCSC Ensembl
Outerchr15:59550283..59641656hg38UCSC Ensembl
Innerchr15:59842519..59933805hg19UCSC Ensembl
Outerchr15:59842482..59933855hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3891374
hg1991374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5507485
SamplesNA20790
Known GenesGCNT3, GTF2A2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668729
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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