A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101156



Internal ID21286365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:209681660..209683343hg38UCSC Ensembl
Innerchr1:209855005..209856688hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg381684
hg191684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110958
Supporting Variants
Samplessample387
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101156
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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