A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1146e199



Internal ID22758919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101034736..101039097hg38UCSC Ensembl
chr6:101482612..101486973hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg384362
hg194362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2658028, esv2657163
SamplesNA19700, NA19703, NA18924, NA18861, NA19819, NA19190, NA19107, NA19379, NA19198, NA19916, NA19138, NA18874, NA19207, NA19172, NA19471, NA18520, NA18908, NA19908, NA19403, NA19152, NA19236, NA19982, NA19114, NA18853, NA18523, NA18858, NA19108, NA19473, NA19444, NA19144, NA19467, NA19248, NA19472, NA19900, NA18511, NA18522, NA18487
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1146e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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