A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv834029



Internal ID16111212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63076461..63224595hg38UCSC Ensembl
Outerchr20:61707813..61855947hg19UCSC Ensembl
Outerchr20:61178258..61326392hg18UCSC Ensembl
Outerchr20:61178258..61326392hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38148135
hg19148135
hg18148135
hg17148135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv68n68
Supporting Variantsnssv1455195, nssv1455221, nssv1455216, nssv1455222, nssv1455204, nssv1455205, nssv1455213, nssv1455209, nssv1455212, nssv1455207, nssv1455219, nssv1455214, nssv1455201, nssv1455215, nssv1455223, nssv1455206, nssv1455208, nssv1455198, nssv1455217, nssv1455218, nssv1455199, nssv1455210, nssv1455203, nssv1455197, nssv1455220, nssv1455211, nssv1455202, nssv1455196, nssv1455200
Samples
Known GenesHAR1A, HAR1B, LOC63930, MIR124-3, YTHDF1
MethodBAC aCGH
AnalysisExperimental SDs (SDautosome) were calculated for each experiment on the basis of the log2 ratios of the 24,392 reliable clones minus the clones removed because of low signal-to-noise ratio (SNR) or high SD of replicate clone measures (SDclone). Thresholds for determining CNV clones were set at a multiple of the SDautosome value. For each experiment, clones were annotated as uninformative if they were filtered via SNR or SDclone, as a CNV loss if the log2 ratio was less than the negative threshold, as unchanged if the log2 ratio was between the negative and positive thresholds, and as a CNV gain if the log2 ratio was above the positive threshold.
PlatformGPL2616
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv834029
Frequency
Sample Size95
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer