A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662964



Internal ID9582383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93511184..93512381hg38UCSC Ensembl
chr9:96273466..96274663hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381198
hg191198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6560062
SamplesHG01488
Known GenesFAM120A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662964
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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