A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669929



Internal ID9589348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7047097..7091663hg38UCSC Ensembl
chr17:6950416..6994982hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3844567
hg1944567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6175424, essv6410038
SamplesNA18986, NA18873
Known GenesCLEC10A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669929
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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