A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2858569



Internal ID10531549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:75352104..75352333hg38UCSC Ensembl
Outerchr10:77111862..77112091hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7128136
SamplesHuRef
Known GenesZNF503-AS1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2858569
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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