A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659056



Internal ID9578475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:159300166..159301220hg38UCSC Ensembl
Outerchr3:159300129..159301270hg38UCSC Ensembl
Innerchr3:159017955..159019009hg19UCSC Ensembl
Outerchr3:159017918..159019059hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg381142
hg191142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5677110
SamplesNA20512
Known GenesIQCJ-SCHIP1, SCHIP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659056
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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