A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv199e180



Internal ID20123138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108900765..108900866hg38UCSC Ensembl
chr9:111663045..111663146hg19UCSC Ensembl
chr9:110702866..110702967hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38102
hg19102
hg18102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv987554, esv1006666
SamplesHuRef
Known GenesIKBKAP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)dgv199e180
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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