A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668879



Internal ID9588298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61273661..61278935hg38UCSC Ensembl
Outerchr17:61273624..61278985hg38UCSC Ensembl
Innerchr17:59351022..59356296hg19UCSC Ensembl
Outerchr17:59350985..59356346hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg385362
hg195362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5638924
SamplesHG00464
Known GenesBCAS3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668879
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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