A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1320e199



Internal ID22759093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5749939..5751598hg38UCSC Ensembl
chr9:5749939..5751598hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381660
hg191660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2671463, esv2670730
SamplesNA19920, NA19471, NA19982, NA19434, NA19444
Known GenesKIAA1432
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1320e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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