A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111774



Internal ID21295040
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 StatusM
Merged Variants
Supporting Variantsnssv14090181
Samplessample149
Known GenesUSP6NL
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111774
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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