A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469650



Internal ID15187679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43901842..44051273hg38UCSC Ensembl
Innerchr19:44405994..44555426hg19UCSC Ensembl
Innerchr19:49097834..49247266hg18UCSC Ensembl
Innerchr19:49097834..49247266hg16UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38149432
hg19149433
hg18149433
hg16149433
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1674401, nssv1672700, nssv1675152, nssv1675880, nssv1674896, nssv1672883, nssv1673005, nssv1673315, nssv1674599, nssv1673766, nssv1673565, nssv1672069, nssv1676637, nssv1672870, nssv1672750
Samples
Known GenesZNF155, ZNF221, ZNF222, ZNF230, ZNF45
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)nsv469650
Frequency
Sample Size265
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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