A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664816



Internal ID9930921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79860573..79860917hg38UCSC Ensembl
chr9:82475488..82475832hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5460793, essv5742661, essv6246178, essv6225014, essv5968959, essv6416895, essv5745950, essv5856715, essv5439468, essv6347943, essv6586087, essv6594974, essv5695165
SamplesNA18508, NA18486, NA19377, NA18510, NA19381, NA19319, NA19382, NA11918, NA18856, NA19099, NA18576, NA19428, NA18505
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664816
Frequency
Sample Size1151
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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