A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7126691



Internal ID10058287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46401763..46477457hg38UCSC Ensembl
Innerchr10:47072000..47148000hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3875695
hg1976001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2857124
Supporting Variants
SamplesHuRef
Known GenesHNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7126691
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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