A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673538



Internal ID9592957
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6210152, essv5999807
SamplesHG00325, HG00116
Known GenesGOLM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673538
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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