A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv35e199



Internal ID22757808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29694338..30506895hg38UCSC Ensembl
chr1:30167185..30979742hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38812558
hg19812558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2668677, esv2657775
SamplesNA18861, NA18592, NA18508, NA11931, NA18603, NA18563, NA20798, NA18498, NA18964, NA19137, NA19238, NA18952, NA18517, NA12763, NA06986, NA19093, NA18505, NA19129, NA18522, NA18965
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv35e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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