A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660491



Internal ID9926596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121752238..121752452hg38UCSC Ensembl
chr9:124514517..124514731hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5870690, essv5429173, essv5796410, essv6588226, essv6327942, essv5656562, essv6152778, essv5890281, essv6265775
SamplesNA18486, NA18519, NA18498, NA19371, HG01047, NA18523, NA19375, NA18517, NA19360
Known GenesDAB2IP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660491
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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