A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090181



Internal ID21270320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11610635..11613858hg38UCSC Ensembl
Innerchr10:11652634..11655857hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383224
hg193224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111774
Supporting Variants
Samplessample149
Known GenesUSP6NL
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090181
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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