A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101457



Internal ID21287016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:178982843..179005655hg38UCSC Ensembl
Innerchr1:178951978..178974790hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3822813
hg1922813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117867
Supporting Variants
Samplessample397
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101457
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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