A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6210152



Internal ID9187555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86081074..86082397hg38UCSC Ensembl
chr9:88695989..88697312hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381324
hg191324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673538
Supporting Variants
SamplesHG00116
Known GenesGOLM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6210152
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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