A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv936e199



Internal ID22758709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40620086..40627470hg38UCSC Ensembl
chr4:40622103..40629487hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg387385
hg197385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2660375, esv2672421
SamplesNA18635
Known GenesRBM47
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv936e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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