A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv568e199



Internal ID20123870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77267821..77277205hg38UCSC Ensembl
chr17:75263903..75273287hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg389385
hg199385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672295, esv2668188
SamplesHG00231, NA20766, NA12341, HG01168, NA19725, HG01101, HG01190, NA20807, NA07056
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv568e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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