A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088945



Internal ID21273312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21474402..21485892hg38UCSC Ensembl
Innerchr10:21763331..21774821hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3811491
hg1911491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110709
Supporting Variants
Samplessample19
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088945
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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