A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7128136



Internal ID10059732
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 StatusS
Merged Variantsesv2858569
Supporting Variants
SamplesHuRef
Known GenesZNF503-AS1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7128136
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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