A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673276



Internal ID9939381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95150262..95156654hg38UCSC Ensembl
chr10:96910019..96916411hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg386393
hg196393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6442446
SamplesNA18631
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673276
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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