A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469794



Internal ID15187823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36638956..36819355hg38UCSC Ensembl
Innerchr19:37129858..37310257hg19UCSC Ensembl
Innerchr19:41821698..42002097hg18UCSC Ensembl
Innerchr19:41821698..42002097hg16UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38180400
hg19180400
hg18180400
hg16180400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672556
Samples
Known GenesZNF461, ZNF567, ZNF790, ZNF790-AS1, ZNF850
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nsv469794
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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