A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6457236



Internal ID9434639
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
SamplesHG00476
Known GenesABCA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6457236
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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