A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662881



Internal ID9582300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46629865..46631296hg38UCSC Ensembl
chr6:46597602..46599033hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg381432
hg191432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6192934
SamplesNA19347
Known GenesCYP39A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662881
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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