A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv36e199



Internal ID22757809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:30286067..30662075hg38UCSC Ensembl
chr1:30758914..31134922hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38376009
hg19376009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2662099, esv2677487
SamplesHG00249, NA11843, HG01061
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv36e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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