A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv938e199



Internal ID22758711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44016273..44025425hg38UCSC Ensembl
chr4:44018290..44027442hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg389153
hg199153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2678664, esv2656939
SamplesNA19700, NA19819, NA20346, NA18870, NA20356, NA19446, NA19315, HG01083, NA20278, NA19383, NA19137, NA20127, NA19908, NA19210, NA19437, HG01171, NA19462, HG01095, NA19391, NA19327, NA20126, NA19114, NA20299, NA18853, NA20282, NA19099, NA19452, NA19318, NA19834, NA19321, NA19256, NA19473, HG01253, NA19380, NA20281, NA19360, NA19818, NA19468, NA19713, NA19102, NA19711, NA19900, NA19430, NA20322
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv938e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss44
Observed Complex0
Frequencyn/a


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