A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7425367



Internal ID10356963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114526438..114526508hg38UCSC Ensembl
chr11:114397160..114397230hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3155800
Supporting Variants
SamplesHuRef
Known GenesNXPE1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7425367
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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