A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5907944



Internal ID8885347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104833906..104834822hg38UCSC Ensembl
chr9:107596187..107597103hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675308
Supporting Variants
SamplesNA19064
Known GenesABCA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5907944
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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