A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1160e199



Internal ID22758933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144326126..144333875hg38UCSC Ensembl
chr6:144647262..144655011hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg387750
hg197750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2657131, esv2676622
SamplesNA19311
Known GenesUTRN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1160e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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