A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670385



Internal ID9589804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48761168..48769231hg38UCSC Ensembl
chr10:49969213..49977276hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg388064
hg198064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5427009
SamplesNA20760
Known GenesWDFY4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670385
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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