A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2844902



Internal ID10864599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67543501..67549861hg38UCSC Ensembl
Innerchr9:65912000..65918360hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg386361
hg196361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7114469
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2844902
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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