A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088494



Internal ID21272054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36703297..36706375hg38UCSC Ensembl
Innerchr10:36992225..36995303hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg383079
hg193079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110678
Supporting Variants
Samplessample171
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088494
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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