A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv29e199



Internal ID22757802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23764964..23773446hg38UCSC Ensembl
chr1:24091454..24099936hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg388483
hg198483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2663043, esv2658633
SamplesNA19350, NA19393, NA19443, NA19446, NA19448, NA19383, NA19452, NA19469, NA19436, NA19440, NA19470, NA19438, NA19468, NA19430, NA19431
Known GenesLOC100506963
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv29e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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