A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1358e199



Internal ID22759131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88515609..88519148hg38UCSC Ensembl
chr9:91130524..91134063hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg383540
hg193540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2674162, esv2675528
SamplesNA19678, HG00657, NA20334
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1358e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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