A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3585568



Internal ID6710264
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 StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006666
Supporting Variants
SamplesHuRef
Known GenesIKBKAP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3585568
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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