A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672095



Internal ID9938200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:81655824..81656533hg38UCSC Ensembl
Outerchr3:81655787..81656583hg38UCSC Ensembl
Innerchr3:81704975..81705684hg19UCSC Ensembl
Outerchr3:81704938..81705734hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38797
hg19797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5883260
SamplesNA18561
Known GenesGBE1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672095
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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