A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1337e199



Internal ID22759110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34726114..34835302hg38UCSC Ensembl
chr9:34726111..34835299hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38109189
hg19109189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2675649, esv2672659
SamplesHG00595, NA19074
Known GenesFAM205A, FAM205B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1337e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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