A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094877



Internal ID21268970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:76919289..76971215hg38UCSC Ensembl
Innerchr1:77384974..77436900hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3851927
hg1951927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117783
Supporting Variants
Samplessample133
Known GenesST6GALNAC5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094877
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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