A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117761



Internal ID21301027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:172420246..172427031hg38UCSC Ensembl
Innerchr1:172389386..172396171hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg386786
hg196786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086539, nssv14094172
Samplessample322, sample163
Known GenesC1orf105
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117761
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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