A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv39e199



Internal ID22757812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39819446..39821568hg38UCSC Ensembl
chr1:40285118..40287240hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg382123
hg192123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2675211, esv2664104
SamplesNA18988
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv39e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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