A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2852680



Internal ID10872377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45784552..45792552hg38UCSC Ensembl
Innerchr10:46280000..46288000hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7122247
SamplesHuRef
Known GenesFAM21C
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2852680
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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