A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661414



Internal ID9927519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83049519..83055592hg38UCSC Ensembl
chr9:85664434..85670507hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg386074
hg196074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5955498, essv5797704, essv6357735, essv6406846, essv6193251, essv6450563, essv5961863, essv6290602, essv6409964, essv5806745, essv6319545
SamplesNA19190, NA18519, NA18498, NA18874, NA19236, NA18871, NA18499, NA19390, NA19900, NA18505, NA20322
Known GenesRASEF
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661414
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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