A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664340



Internal ID9583759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90842186..90842485hg38UCSC Ensembl
Outerchr9:90842147..90842542hg38UCSC Ensembl
Innerchr9:93604468..93604767hg19UCSC Ensembl
Outerchr9:93604429..93604824hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5699046, essv5858591, essv5571542, essv5856636, essv5727388, essv6084231, essv5802323, essv6067151, essv5754317, essv6250424, essv6331946, essv5686381, essv5812411, essv5876529
SamplesNA12383, HG00142, NA12273, HG00138, NA19720, HG00149, HG00266, NA19655, HG00126, NA19434, NA19072, NA19835, NA19470, HG00112
Known GenesSYK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664340
Frequency
Sample Size1151
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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