A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101915



Internal ID21285830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161414072..161421902hg38UCSC Ensembl
Innerchr1:161383862..161391692hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg387831
hg197831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112541
Supporting Variants
Samplessample38
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101915
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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