A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620966



Internal ID7007836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86832287..86839713hg38UCSC Ensembl
Innerchr9:86832316..86839685hg38UCSC Ensembl
Outerchr9:86832259..86839742hg38UCSC Ensembl
chr9:89447202..89454628hg19UCSC Ensembl
Innerchr9:89447231..89454600hg19UCSC Ensembl
Outerchr9:89447174..89454657hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387427
hg197427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13546869, essv13546873, essv13546871, essv13546870, essv13546876, essv13546872, essv13546874, essv13546875
SamplesHG00361, HG00356, HG00182, HG03653, HG00254, HG01111, HG00345, NA21120
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620966
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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